Daae (-Finsen) disease(epidemic pleurodynia)   B33.0

Da Costa's syndrome   F45.8

Dabney's grip   B33.0

Dacryoadenitis, dacryadenitis   H04.00-

acute   H04.01-

chronic   H04.02-

Dacryocystitis   H04.30-

acute   H04.32-

chronic   H04.41-

neonatal   P39.1

phlegmonous   H04.31-

syphilitic   A52.71

congenital(early)   A50.01

trachomatous, active   A71.1

sequelae(late effect)   B94.0

Dacryocystoblenorrhea- see Inflammation, lacrimal, passages, chronic

Dacryocystocele- see Disorder, lacrimal system, changes

Dacryolith, dacryolithiasis   H04.51-

Dacryoma- see Disorder, lacrimal system, changes

Dacryopericystitis- see Dacryocystitis

Dacryops   H04.11-

Dacryostenosis - see also Stenosis, lacrimal

congenital   Q10.5

Dactylitis

bone- see Osteomyelitis

sickle-cell   D57.00

Hb C   D57.219

Hb SS   D57.00

specified NEC   D57.819

skin   L08.9

syphilitic   A52.77

tuberculous   A18.03

Dactylolysis spontanea(ainhum)   L94.6

Dactylosymphysis   Q70.9

fingers- see Syndactylism, complex, fingers

toes- see Syndactylism, complex, toes

Damage

arteriosclerotic- see Arteriosclerosis

brain(nontraumatic)   G93.9

anoxic, hypoxic   G93.1

resulting from a procedure   G97.82

child NEC   G80.9

due to birth injury   P11.2

cardiorenal(vascular) - see Hypertension, cardiorenal

cerebral NEC- see Damage, brain

coccyx, complicating delivery   O71.6

coronary- see Disease, heart, ischemic

deep tissue, pressure-induced - see also L89 with final character .6

eye, birth injury   P15.3

liver(nontraumatic)   K76.9

alcoholic   K70.9

due to drugs- see Disease, liver, toxic

toxic- see Disease, liver, toxic

lung

dabbing(related)   U07.0

electronic cigarette(related)   U07.0

vaping(associated) (device) (product) (use)   U07.0

medication   T88.7

organ

dabbing(related)   U07.0

electronic cigarette(related)   U07.0

vaping(associated) (device) (product) (use)   U07.0

pelvic

joint or ligament, during delivery   O71.6

organ NEC

during delivery   O71.5

following ectopic or molar pregnancy   O08.6

renal- see Disease, renal

subendocardium, subendocardial- see Degeneration, myocardial

vascular   I99.9

Dana-Putnam syndrome(subacute combined sclerosis with pernicious anemia) - see Degeneration, combined

Danbolt(-Cross) syndrome(acrodermatitis enteropathica)   E83.2

Dandruff   L21.0

Dandy-Walker syndrome   Q03.1

with spina bifida- see Spina bifida

Danlos' syndrome - see also Syndrome, Ehlers-Danlos   Q79.60

Darier(-White) disease(congenital)   Q82.8

meaning erythema annulare centrifugum   L53.1

Darier-Roussy sarcoid   D86.3

Darling's disease or histoplasmosis   B39.4

Darwin's tubercle   Q17.8

Dawson's (inclusion body) encephalitis   A81.1

De Beurmann (-Gougerot) disease   B42.1

De la Tourette's syndrome   F95.2

De Lange's syndrome   Q87.19

De Morgan's spots(senile angiomas)   I78.1

De Quervain's

disease(tendon sheath)   M65.4

syndrome   E34.51

thyroiditis(subacute granulomatous thyroiditis)   E06.1

De Toni-Fanconi (-Debré) syndrome   E72.09

with cystinosis   E72.04

Dead

fetus, retained(mother)   O36.4

early pregnancy   O02.1

labyrinth- see subcategory H83.2

ovum, retained   O02.0

Deaf nonspeaking NEC   H91.3

Deafmutism (acquired) (congenital) NEC   H91.3

hysterical   F44.6

syphilitic, congenital - see also subcategory H94.8   A50.09

Deafness(acquired) (complete) (hereditary) (partial)   H91.9-

with blue sclera and fragility of bone   Q78.0

auditory fatigue- see Deafness, specified type NEC

aviation   T70.0

nerve injury- see Injury, nerve, acoustic, specified type NEC

boilermaker's- see subcategory H83.3

central- see Deafness, sensorineural

conductive   H90.2

and sensorineural

mixed   H90.8

bilateral   H90.6

bilateral   H90.0

unilateral   H90.1-

with restricted hearing on the contralateral side   H90.A-

congenital   H90.5

with blue sclera and fragility of bone   Q78.0

due to toxic agents- see Deafness, ototoxic

emotional(hysterical)   F44.6

functional(hysterical)   F44.6

high frequency   H91.9-

hysterical   F44.6

low frequency   H91.9-

mental   R48.8

mixed conductive and sensorineural   H90.8

bilateral   H90.6

unilateral   H90.7-

nerve- see Deafness, sensorineural

neural- see Deafness, sensorineural

noise-induced - see also subcategory   H83.3

nerve injury- see Injury, nerve, acoustic, specified type NEC

nonspeaking   H91.3

ototoxic- see subcategory H91.0

perceptive- see Deafness, sensorineural

psychogenic(hysterical)   F44.6

sensorineural   H90.5

and conductive

mixed   H90.8

bilateral   H90.6

bilateral   H90.3

unilateral   H90.4-

with restricted hearing on the contralateral side   H90.A-

sensory- see Deafness, sensorineural

specified type NEC- see subcategory H91.8

sudden(idiopathic)   H91.2-

syphilitic   A52.15

transient ischemic   H93.01-

traumatic- see Injury, nerve, acoustic, specified type NEC

word(developmental)   H93.25

Death(cause unknown) (of) (unexplained) (unspecified cause)   R99

brain   G93.82

cardiac(sudden) (with successful resuscitation) - see Arrest, cardiac

family history of   Z82.41

personal history of   Z86.74

family member(assumed)   Z63.4

Debility(chronic) (general) (nervous)   R53.81

congenital or neonatal NOS   P96.9

nervous   R53.81

old age   R54

senile   R54

Débove's disease(splenomegaly)   R16.1

Debt, burdensome   Z59.86

Decalcification

bone- see Osteoporosis

teeth   K03.89

Decapsulation, kidney   N28.89

Decay

dental- see Caries, dental

senile   R54

tooth, teeth- see Caries, dental

Deciduitis(acute)

following ectopic or molar pregnancy   O08.0

Decline(general) - see Debility

cognitive, age-associated   R41.81

Decompensation

cardiac(acute) (chronic) - see Disease, heart

cardiovascular- see Disease, cardiovascular

heart- see Disease, heart

hepatic- see Failure, hepatic

myocardial(acute) (chronic) - see Disease, heart

respiratory   J98.8

Decompression sickness   T70.3

Decrease(d)

absolute neutrophile count- see Neutropenia

blood

platelets- see Thrombocytopenia

pressure   R03.1

due to shock following

injury   T79.4

operation   T81.19

estrogen   E28.39

postablative   E89.40

asymptomatic   E89.40

symptomatic   E89.41

fragility of erythrocytes   D58.8

function

lipase(pancreatic)   K90.3

ovary in hypopituitarism   E23.0

parenchyma of pancreas   K86.89

pituitary(gland) (anterior) (lobe)   E23.0

posterior(lobe)   E23.0

functional activity   R68.89

glucose   R73.09

hematocrit   R71.0

hemoglobin   R71.0

leukocytes   D72.819

specified NEC   D72.818

libido   R68.82

lymphocytes   D72.810

platelets   D69.6

respiration, due to shock following injury   T79.4

sexual desire   R68.82

tear secretion NEC- see Syndrome, dry eye

tolerance

fat   K90.49

glucose   R73.09

pancreatic   K90.3

salt and water   E87.8

vision NEC   H54.7

white blood cell count   D72.819

specified NEC   D72.818

Decubitus(ulcer) - see Ulcer, pressure, by site

cervix   N86

Deepening acetabulum- see Derangement, joint, specified type NEC, hip

Defect, defective   Q89.9

3-beta-hydroxysteroid dehydrogenase   E25.0

11-hydroxylase   E25.0

21-hydroxylase   E25.0

abdominal wall, congenital   Q79.59

antibody immunodeficiency   D80.9

aorticopulmonary septum   Q21.4

atrial septal   Q21.10

coronary sinus   Q21.13

following acute myocardial infarction(current complication)   I23.1

ostium primum type(type I)   Q21.20

with

common atrioventricular valves and moderate or larger inlet VSD   Q21.23

separate atrioventricular valves   Q21.21

and small or restrictive inlet VSD   Q21.22

ostium secundum type(patent persistent) (type II)   Q21.11

sinus venosus   Q21.16

inferior   Q21.15

superior   Q21.14

specified NEC   Q21.19

vena cava type

inferior   Q21.15

superior   Q21.14

atrioventricular

canal   Q21.20

septal

common   Q21.23

complete   Q21.23

incomplete   Q21.21

intermediate   Q21.22

partial   Q21.21

transitional   Q21.22

unspecified as to partial or complete   Q21.20

septum   Q21.20

auricular septal   Q21.10

bilirubin excretion NEC   E80.6

biosynthesis, androgen(testicular)   E29.1

bulbar septum   Q21.0

catalase   E80.3

cell membrane receptor complex(CR3)   D71

circulation   I99.9

congenital   Q28.9

newborn   Q28.9

coagulation(factor) - see also Deficiency, factor   D68.9

with

ectopic pregnancy   O08.1

molar pregnancy   O08.1

acquired   D68.4

antepartum with hemorrhage- see Hemorrhage, antepartum, with coagulation defect

due to

liver disease   D68.4

vitamin K deficiency   D68.4

hereditary NEC   D68.2

intrapartum   O67.0

newborn, transient   P61.6

postpartum   O99.13

with hemorrhage   O72.3

specified type NEC   D68.8

complement system   D84.1

conduction(heart)   I45.9

bone- see Deafness, conductive

congenital, organ or site not listed- see Anomaly, by site

coronary sinus   Q21.13

cushion, endocardial   Q21.20

common   Q21.23

incomplete   Q21.21

intermediate   Q21.22

transitional   Q21.22

degradation, glycoprotein   E77.1

dental bridge, crown, fillings- see Defect, dental restoration

dental restoration   K08.50

specified NEC   K08.59

dentin(hereditary)   K00.5

Descemet's membrane, congenital   Q13.89

developmental - see also Anomaly

cauda equina   Q06.3

diaphragm

with elevation, eventration or hernia- see Hernia, diaphragm

congenital   Q79.1

with hernia   Q79.0

gross(with hernia)   Q79.0

ectodermal, congenital   Q82.9

Eisenmenger's   Q21.8

enzyme

catalase   E80.3

peroxidase   E80.3

esophagus, congenital   Q39.9

extensor retinaculum   M62.89

fibrin polymerization   D68.2

filling

bladder   R93.41

kidney   R93.42-

renal pelvis   R93.41

stomach   R93.3

ureter   R93.41

urinary organs, specified NEC   R93.49

GABA (gamma aminobutyric acid) metabolic   E72.81

Gerbode   Q21.0

glucose transport, blood-brain barrier   E74.810

glycoprotein degradation   E77.1

Hageman(factor)   D68.2

hearing- see Deafness

high grade   F70

home, technical, preventing adequate care   Z59.19

interatrial septal   Q21.19

interauricular septal   Q21.19

interventricular septal   Q21.0

with dextroposition of aorta, pulmonary stenosis and hypertrophy of right ventricle   Q21.3

in tetralogy of Fallot   Q21.3

intervertebral annular fibrosis - see also Disease, intervertebral disc, by site   M51.9

lumbar   M51.A0

large   M51.A2

small   M51.A1

lumbosacral   M51.A3

large   M51.A5

small   M51.A4

learning(specific) - see Disorder, learning

lymphocyte function antigen-1(LFA-1)   D84.0

lysosomal enzyme, post-translational modification   E77.0

major osseous   M89.70

ankle   M89.77-

carpus   M89.74-

clavicle   M89.71-

femur   M89.75-

fibula   M89.76-

fingers   M89.74-

foot   M89.77-

forearm   M89.73-

hand   M89.74-

humerus   M89.72-

lower leg   M89.76-

metacarpus   M89.74-

metatarsus   M89.77-

multiple sites   M89.79

pelvic region   M89.75-

pelvis   M89.75-

radius   M89.73-

scapula   M89.71-

shoulder region   M89.71-

specified NEC   M89.78

tarsus   M89.77-

thigh   M89.75-

tibia   M89.76-

toes   M89.77-

ulna   M89.73-

mental- see Disability, intellectual

modification, lysosomal enzymes, post-translational   E77.0

obstructive, congenital

renal pelvis   Q62.39

ureter   Q62.39

atresia- see Atresia, ureter

cecoureterocele   Q62.32

megaureter   Q62.2

orthotopic ureterocele   Q62.31

osseous, major   M89.70

ankle   M89.77-

carpus   M89.74-

clavicle   M89.71-

femur   M89.75-

fibula   M89.76-

fingers   M89.74-

foot   M89.77-

forearm   M89.73-

hand   M89.74-

humerus   M89.72-

lower leg   M89.76-

metacarpus   M89.74-

metatarsus   M89.77-

multiple sites   M89.9

pelvic region   M89.75-

pelvis   M89.75-

radius   M89.73-

scapula   M89.71-

shoulder region   M89.71-

specified NEC   M89.78

tarsus   M89.77-

thigh   M89.75-

tibia   M89.76-

toes   M89.77-

ulna   M89.73-

osteochondral NEC - see also Deformity   M95.8

ostium

primum   Q21.20

secundum   Q21.11

peroxidase   E80.3

placental blood supply- see Insufficiency, placental

platelets, qualitative   D69.1

constitutional- see Disease, von Willebrand

postural NEC, spine- see Dorsopathy, deforming

qualitative, of von Willebrand factor

with

decreased platelet adhesion and selective deficiency of high-molecular-weight multimers - see also Disease, von Willebrand   D68.020

defective platelet adhesion with a normal size distribution of von Willebrand factor multimers - see also Disease, von Willebrand   D68.022

defective von Willebrand factor to factor VIII binding - see also Disease, von Willebrand   D68.023

high-molecular-weight von Willebrand factor loss - see also Disease, von Willebrand   D68.021

hyper-adhesive forms - see also Disease, von Willebrand   D68.021

increased affinity for platelet glycoprotein lb - see also Disease, von Willebrand   D68.021

markedly decreased affinity for factor VIII - see also Disease, von Willebrand   D68.023

in von Willebrand factor function, with no further subtyping - see also Disease, von Willebrand   D68.029

reduction

limb   Q73.8

lower   Q72.9-

absence- see Agenesis, leg

foot- see Agenesis, foot

longitudinal

femur   Q72.4-

fibula   Q72.6-

tibia   Q72.5-

specified type NEC   Q72.89-

split foot   Q72.7-

specified type NEC   Q73.8

upper   Q71.9-

absence- see Agenesis, arm

forearm- see Agenesis, forearm

hand- see Agenesis, hand

lobster-claw hand   Q71.6-

longitudinal

radius   Q71.4-

ulna   Q71.5-

specified type NEC   Q71.89-

renal pelvis   Q63.8

obstructive   Q62.39

respiratory system, congenital   Q34.9

restoration, dental   K08.50

specified NEC   K08.59

retinal nerve bundle fibers   H35.89

septal (heart) NOS   Q21.9

acquired(atrial) (auricular) (ventricular) (old)   I51.0

atrial - see also Defect, atrial septal   Q21.10

concurrent with acute myocardial infarction- see Infarct, myocardium

following acute myocardial infarction(current complication)   I23.1

ventricular - see also Defect, ventricular septal   Q21.0

sinus venosus - see also Defect, atrial septal, sinus venosus   Q21.16

speech- see Disorder, speech

developmental   F80.9

specified NEC   R47.89

Taussig-Bing(aortic transposition and overriding pulmonary artery)   Q20.1

teeth, wedge   K03.1

vascular(local)   I99.9

congenital   Q27.9

ventricular septal   Q21.0

concurrent with acute myocardial infarction- see Infarct, myocardium

following acute myocardial infarction(current complication)   I23.2

in tetralogy of Fallot   Q21.3

vision NEC   H54.7

visual field   H53.40

bilateral

heteronymous   H53.47

homonymous   H53.46-

generalized contraction   H53.48-

localized

arcuate   H53.43-

scotoma(central area)   H53.41-

blind spot area   H53.42-

sector   H53.43-

specified type NEC   H53.45-

voice   R49.9

specified NEC   R49.8

wedge, tooth, teeth(abrasion)   K03.1

Deferentitis   N49.1

gonorrheal(acute) (chronic)   A54.23

Defibrination(syndrome)   D65

antepartum- see Hemorrhage, antepartum, with coagulation defect, disseminated intravascular coagulation

following ectopic or molar pregnancy   O08.1

intrapartum   O67.0

newborn   P60

postpartum   O72.3

Deficiency, deficient

3-beta hydroxysteroid dehydrogenase   E25.0

5-alpha reductase(with male pseudohermaphroditism)   E29.1

11-hydroxylase   E25.0

21-hydroxylase   E25.0

AADC(aromatic L-amino acid decarboxylase)   E70.81

abdominal muscle syndrome   Q79.4

accelerator globulin(Ac G) (blood)   D68.2

AC globulin(congenital) (hereditary)   D68.2

acquired   D68.4

acid phosphatase   E83.39

acid sphingomyelinase(ASMD)   E75.249

type

A   E75.240

A/B   E75.244

B   E75.241

activating factor(blood)   D68.2

ADA2(adenosine deaminase 2)   D81.32

adenosine deaminase(ADA)   D81.30

with severe combined immunodeficiency(SCID)   D81.31

partial(type 1)   D81.39

specified NEC   D81.39

type 1(without SCID) (without severe combined immunodeficiency)   D81.39

type 2   D81.32

aldolase(hereditary)   E74.19

alpha-1-antitrypsin   E88.01

amino-acids   E72.9

anemia- see Anemia

aneurin   E51.9

antibody with

hyperimmunoglobulinemia   D80.6

near-normal immunoglobins   D80.6

antidiuretic hormone   E23.2

anti-hemophilic

factor(A)   D66

B   D67

C   D68.1

globulin (AHG) NEC   D66

antithrombin(antithrombin III)   D68.59

aromatic L-amino acid decarboxylase(AADC)   E70.81

ascorbic acid   E54

attention(disorder) (syndrome)   F98.8

with hyperactivity- see Disorder, attention-deficit hyperactivity

autoprothrombin

I   D68.2

II   D67

C   D68.2

beta-glucuronidase   E76.29

biotin   E53.8

biotin-dependent carboxylase   D81.819

biotinidase   D81.810

brancher enzyme(amylopectinosis)   E74.03

calciferol   E55.9

with

adult osteomalacia   M83.8

rickets- see Rickets

calcium(dietary)   E58

calorie, severe   E43

with marasmus   E41

and kwashiorkor   E42

cardiac- see Insufficiency, myocardial

carnitine   E71.40

due to

hemodialysis   E71.43

inborn errors of metabolism   E71.42

Valproic acid therapy   E71.43

iatrogenic   E71.43

muscle palmityltransferase   E71.314

primary   E71.41

secondary   E71.448

carotene   E50.9

central nervous system   G96.89

ceruloplasmin(Wilson)   E83.01

choline   E53.8

Christmas factor   D67

chromium   E61.4

chronic neurovisceral acid sphingomyelinase   E75.244

chronic visceral acid sphingomyelinase   E75.241

clotting(blood) - see also Deficiency, coagulation factor   D68.9

clotting factor NEC(hereditary) - see also Deficiency, factor   D68.2

coagulation NOS   D68.9

with

ectopic pregnancy   O08.1

molar pregnancy   O08.1

acquired(any)   D68.4

antepartum hemorrhage- see Hemorrhage, antepartum, with coagulation defect

clotting factor NEC - see also Deficiency, factor   D68.2

due to

hyperprothrombinemia   D68.4

liver disease   D68.4

vitamin K deficiency   D68.4

newborn, transient   P61.6

postpartum   O72.3

specified NEC   D68.8

cognitive   F09

color vision   H53.50

achromatopsia   H53.51

acquired   H53.52

deuteranomaly   H53.53

protanomaly   H53.54

specified type NEC   H53.59

tritanomaly   H53.55

combined glucocorticoid and mineralocorticoid   E27.49

contact factor   D68.2

copper(nutritional)   E61.0

corticoadrenal   E27.40

primary   E27.1

craniofacial axis   Q75.0

cyanocobalamin   E53.8

C1 esterase inhibitor(C1-INH)   D84.1

debrancher enzyme(limit dextrinosis)   E74.03

dehydrogenase

long chain/very long chain acyl CoA   E71.310

medium chain acyl CoA   E71.311

short chain acyl CoA   E71.312

diet   E63.9

dihydropyrimidine dehydrogenase(DPD)   E88.89

disaccharidase   E73.9

edema- see Malnutrition, severe

endocrine   E34.9

energy-supply- see Malnutrition

enzymes, circulating NEC   E88.09

ergosterol   E55.9

with

adult osteomalacia   M83.8

rickets- see Rickets

essential fatty acid(EFA)   E63.0

eye movements

saccadic   H55.81

smooth pursuit   H55.82

factor - see also Deficiency, coagulation

Hageman   D68.2

I(congenital) (hereditary)   D68.2

II(congenital) (hereditary)   D68.2

IX(congenital) (functional) (hereditary) (with functional defect)   D67

multiple(congenital)   D68.8

acquired   D68.4

V(congenital) (hereditary)   D68.2

VII(congenital) (hereditary)   D68.2

VIII(congenital) (functional) (hereditary) (with functional defect)   D66

with vascular defect- see Disease, von Willebrand

X(congenital) (hereditary)   D68.2

XI(congenital) (hereditary)   D68.1

XII(congenital) (hereditary)   D68.2

XIII(congenital) (hereditary)   D68.2

femoral, proximal focal(congenital) - see Defect, reduction, lower limb, longitudinal, femur

fibrin-stabilizing factor(congenital) (hereditary)   D68.2

acquired   D68.4

fibrinase   D68.2

fibrinogen(congenital) (hereditary)   D68.2

acquired   D65

folate   E53.8

folic acid   E53.8

foreskin   N47.3

fructokinase   E74.11

fructose 1,6-diphosphatase   E74.19

fructose-1-phosphate aldolase   E74.19

GABA (gamma aminobutyric acid) transaminase   E72.81

GABA-T(gamma aminobutyric acid transaminase)   E72.81

galactokinase   E74.29

galactose-1-phosphate uridyl transferase   E74.29

gammaglobulin in blood   D80.1

hereditary   D80.0

glass factor   D68.2

glucocorticoid   E27.49

mineralocorticoid   E27.49

glucose-6-phosphatase   E74.01

glucose-6-phosphate dehydrogenase

anemia   D55.0

without anemia   D75.A

glucose transporter protein type 1   E74.810

glucuronyl transferase   E80.5

Glut1   E74.810

glycogen synthetase   E74.09

gonadotropin(isolated)   E23.0

growth hormone(idiopathic) (isolated)   E23.0

Hageman factor   D68.2

hemoglobin   D64.9

hepatophosphorylase   E74.09

homogentisate 1,2-dioxygenase   E70.29

hormone

anterior pituitary (partial) NEC   E23.0

growth   E23.0

growth(isolated)   E23.0

pituitary   E23.0

testicular   E29.1

hypoxanthine-(guanine)-phosphoribosyltransferase (HG- PRT) (total H-PRT)   E79.1

immunity   D84.9

cell-mediated   D84.89

with thrombocytopenia and eczema   D82.0

combined   D81.9

humoral   D80.9

IgA(secretory)   D80.2

IgG   D80.3

IgM   D80.4

immuno- see Immunodeficiency

immunoglobulin, selective

A(IgA)   D80.2

G(IgG) (subclasses)   D80.3

M(IgM)   D80.4

infantile neurovisceral acid sphingomyelinase   E75.240

inositol(B complex)   E53.8

intrinsic

factor(congenital)   D51.0

sphincter   N36.42

with urethral hypermobility   N36.43

iodine   E61.8

congenital syndrome- see Syndrome, iodine-deficiency, congenital

iron   E61.1

anemia   D50.9

kalium   E87.6

kappa-light chain   D80.8

labile factor(congenital) (hereditary)   D68.2

acquired   D68.4

lacrimal fluid(acquired) - see also Syndrome, dry eye

congenital   Q10.6

lactase

congenital   E73.0

secondary   E73.1

Laki-Lorand factor   D68.2

lecithin cholesterol acyltransferase   E78.6

lipocaic   K86.89

lipoprotein(familial) (high density)   E78.6

liver phosphorylase   E74.09

lysosomal alpha-1, 4 glucosidase   E74.02

magnesium   E61.2

major histocompatibility complex

class I   D81.6

class II   D81.7

manganese   E61.3

menadione(vitamin K)   E56.1

newborn   P53

mental(familial) (hereditary) - see Disability, intellectual

methylenetetrahydrofolate reductase(MTHFR)   E72.12

mevalonate kinase   M04.1

mineral NEC   E61.8

mineralocorticoid   E27.49

with glucocorticoid   E27.49

molybdenum(nutritional)   E61.5

moral   F60.2

multiple nutrient elements   E61.7

multiple sulfatase(MSD)   E75.26

muscle

carnitine(palmityltransferase)   E71.314

phosphofructokinase   E74.09

myoadenylate deaminase   E79.2

myocardial- see Insufficiency, myocardial

myophosphorylase   E74.04

NADH diaphorase or reductase(congenital)   D74.0

NADH-methemoglobin reductase(congenital)   D74.0

natrium   E87.1

niacin(amide) (-tryptophan)   E52

nicotinamide   E52

nicotinic acid   E52

number of teeth- see Anodontia

nutrient element   E61.9

multiple   E61.7

specified NEC   E61.8

nutrition, nutritional - see also Nutrition deficient   E63.9

sequelae- see Sequelae, nutritional deficiency

specified NEC   E63.8

of interleukin 1 receptor antagonist[DIRA]   M04.8

ornithine transcarbamylase   E72.4

ovarian   E28.39

oxygen- see Anoxia

pantothenic acid   E53.8

parathyroid(gland)   E20.9

perineum(female)   N81.89

phenylalanine hydroxylase   E70.1

phosphoenolpyruvate carboxykinase   E74.4

phosphofructokinase   E74.19

phosphomannomutuse   E74.818

phosphomannose isomerase   E74.818

phosphomannosyl mutase   E74.818

phosphorylase kinase, liver   E74.09

pituitary hormone(isolated)   E23.0

plasma thromboplastin

antecedent(PTA)   D68.1

component(PTC)   D67

plasminogen(type 1) (type 2)   E88.02

platelet NEC   D69.1

constitutional- see Disease, von Willebrand

polyglandular   E31.8

autoimmune   E31.0

potassium(K)   E87.6

prepuce   N47.3

proaccelerin(congenital) (hereditary)   D68.2

acquired   D68.4

proconvertin factor(congenital) (hereditary)   D68.2

acquired   D68.4

protein - see also Malnutrition   E46

anemia   D53.0

C   D68.59

S   D68.59

prothrombin(congenital) (heredItary)   D68.2

acquired   D68.4

Prower factor   D68.2

pseudocholinesterase   E88.09

PTA(plasma thromboplastin antecedent)   D68.1

PTC(plasma thromboplastin component)   D67

purine nucleoside phosphorylase(PNP)   D81.5

pyracin(alpha) (beta)   E53.1

pyridoxal   E53.1

pyridoxamine   E53.1

pyridoxine(derivatives)   E53.1

pyruvate

carboxylase   E74.4

dehydrogenase   E74.4

riboflavin(vitamin B2)   E53.0

salt   E87.1

secretion

ovary   E28.39

salivary gland(any)   K11.7

urine   R34

selenium(dietary)   E59

serum antitrypsin, familial   E88.01

short stature homeobox gene(SHOX)

with

dyschondrosteosis   Q78.8

short stature(idiopathic)   E34.328

Turner's syndrome   Q96.9

sodium(Na)   E87.1

SPCA(factor VII)   D68.2

sphincter, intrinsic   N36.42

with urethral hypermobility   N36.43

stable factor(congenital) (hereditary)   D68.2

acquired   D68.4

Stuart-Prower(factor X)   D68.2

succinic semialdehyde dehydrogenase   E72.81

sucrase   E74.39

sulfatase   E75.26

sulfite oxidase   E72.19

thiamin, thiaminic(chloride)   E51.9

beriberi(dry)   E51.11

wet   E51.12

thrombokinase   D68.2

newborn   P53

thyroid(gland) - see Hypothyroidism

tocopherol   E56.0

tooth bud   K00.0

transcobalamine II(anemia)   D51.2

vanadium   E61.6

vascular   I99.9

vasopressin   E23.2

vertical ridge   K06.8

viosterol- see Deficiency, calciferol

vitamin (multiple) NOS   E56.9

A   E50.9

with

Bitot's spot(corneal)   E50.1

follicular keratosis   E50.8

keratomalacia   E50.4

manifestations NEC   E50.8

night blindness   E50.5

scar of cornea, xerophthalmic   E50.6

xeroderma   E50.8

xerophthalmia   E50.7

xerosis

conjunctival   E50.0

and Bitot's spot   E50.1

cornea   E50.2

and ulceration   E50.3

sequelae   E64.1

B (complex) NOS   E53.9

with

beriberi(dry)   E51.11

wet   E51.12

pellagra   E52

B1 NOS   E51.9

beriberi(dry)   E51.11

with circulatory system manifestations   E51.11

wet   E51.12

B12   E53.8

B2(riboflavin)   E53.0

B6   E53.1

C   E54

sequelae   E64.2

D   E55.9

with

adult osteomalacia   M83.8

rickets- see Rickets

25-hydroxylase   E83.32

E   E56.0

folic acid   E53.8

G   E53.0

group B   E53.9

specified NEC   E53.8

H(biotin)   E53.8

K   E56.1

of newborn   P53

nicotinic   E52

P   E56.8

PP(pellagra-preventing)   E52

specified NEC   E56.8

thiamin   E51.9

beriberi- see Beriberi

von Willebrand factor

partial quantitative - see also Disease, von Willebrand   D68.01

total quantitative - see also Disease, von Willebrand   D68.03

zinc, dietary   E60

Deficit - see also Deficiency

attention and concentration   R41.840

following

cerebral infarction   I69.310

cerebrovascular disease   I69.910

specified disease NEC   I69.810

nontraumatic

intracerebral hemorrhage   I69.110

specified intracranial hemorrhage NEC   I69.210

subarachnoid hemorrhage   I69.010

disorder- see Attention, deficit

cognitive

communication   R41.841

emotional

following

cerebral infarction   I69.315

cerebrovascular disease   I69.915

specified disease NEC   I69.815

nontraumatic

intracerebral hemorrhage   I69.115

specified intracranial hemorrhage NEC   I69.215

subarachnoid hemorrhage   I69.015

following

cerebral infarction   I69.319

cerebrovascular disease   I69.919

specified disease NEC   I69.819

nontraumatic

intracerebral hemorrhage   I69.119

specified intracranial hemorrhage NEC   I69.219

subarachnoid hemorrhage   I69.019

social

following

cerebral infarction   I69.315

cerebrovascular disease   I69.915

specified disease NEC   I69.815

nontraumatic

intracerebral hemorrhage   I69.115

specified intracranial hemorrhage NEC   I69.215

subarachnoid hemorrhage   I69.015

cognitive NEC   R41.89

following

cerebral infarction   I69.318

cerebrovascular disease   I69.918

specified disease NEC   I69.818

nontraumatic

intracerebral hemorrhage   I69.118

specified intracranial hemorrhage NEC   I69.218

subarachnoid hemorrhage   I69.018

concentration   R41.840

executive function   R41.844

following

cerebral infarction   I69.314

cerebrovascular disease   I69.914

specified disease NEC   I69.814

nontraumatic

intracerebral hemorrhage   I69.114

specified intracranial hemorrhage NEC   I69.214

subarachnoid hemorrhage   I69.014

frontal lobe   R41.844

following

cerebral infarction   I69.314

cerebrovascular disease   I69.914

specified disease NEC   I69.814

nontraumatic

intracerebral hemorrhage   I69.114

specified intracranial hemorrhage NEC   I69.214

subarachnoid hemorrhage   I69.014

memory

following

cerebral infarction   I69.311

cerebrovascular disease   I69.911

specified disease NEC   I69.811

nontraumatic

intracerebral hemorrhage   I69.111

specified intracranial hemorrhage NEC   I69.211

subarachnoid hemorrhage   I69.011

neurologic NEC   R29.818

ischemic

reversible(RIND)   I63.9

prolonged(PRIND)   I63.9

oxygen   R09.02

prolonged reversible ischemic neurologic(PRIND)   I63.9

psychomotor   R41.843

following

cerebral infarction   I69.313

cerebrovascular disease   I69.913

specified disease NEC   I69.813

nontraumatic

intracerebral hemorrhage   I69.113

specified intracranial hemorrhage NEC   I69.213

subarachnoid hemorrhage   I69.013

visuospatial   R41.842

following

cerebral infarction   I69.312

cerebrovascular disease   I69.912

specified disease NEC   I69.812

nontraumatic

intracerebral hemorrhage   I69.112

specified intracranial hemorrhage NEC   I69.212

subarachnoid hemorrhage   I69.012

Deflection

radius- see Deformity, limb, specified type NEC, forearm

septum(acquired) (nasal) (nose)   J34.2

spine- see Curvature, spine

turbinate(nose)   J34.2

Defluvium

capillorum- see Alopecia

ciliorum- see Madarosis

unguium   L60.8

Deformity   Q89.9

abdomen, congenital   Q89.9

abdominal wall

acquired   M95.8

congenital   Q79.59

acquired(unspecified site)   M95.9

adrenal gland   Q89.1

alimentary tract, congenital   Q45.9

upper   Q40.9

ankle(joint) (acquired) - see also Deformity, limb, lower leg

abduction- see Contraction, joint, ankle

congenital   Q68.8

contraction- see Contraction, joint, ankle

specified type NEC- see Deformity, limb, foot, specified NEC

anus(acquired)   K62.89

congenital   Q43.9

aorta(arch) (congenital)   Q25.40

acquired   I77.89

aortic

arch, acquired   I77.89

cusp or valve(congenital)   Q23.8

acquired - see also Endocarditis, aortic   I35.8

arm(acquired) (upper) - see also Deformity, limb, upper arm

congenital   Q68.8

forearm- see Deformity, limb, forearm

artery (congenital) (peripheral) NOS   Q27.9

acquired   I77.89

coronary(acquired)   I25.9

congenital   Q24.5

umbilical   Q27.0

atrial septal - see also Defect, atrial septal   Q21.10

auditory canal(external) (congenital) - see also Malformation, ear, external

acquired- see Disorder, ear, external, specified type NEC

auricle

ear(congenital) - see also Malformation, ear, external

acquired- see Disorder, pinna, deformity

back- see Dorsopathy, deforming

bile duct(common) (congenital) (hepatic)   Q44.5

acquired   K83.8

biliary duct or passage(congenital)   Q44.5

acquired   K83.8

bladder(neck) (trigone) (sphincter) (acquired)   N32.89

congenital   Q64.79

bone (acquired) NOS   M95.9

congenital   Q79.9

turbinate   M95.0

brain(congenital)   Q04.9

acquired   G93.89

reduction   Q04.3

breast(acquired)   N64.89

congenital   Q83.9

reconstructed   N65.0

bronchus(congenital)   Q32.4

acquired NEC   J98.09

bursa, congenital   Q79.9

canaliculi(lacrimalis) (acquired) - see also Disorder, lacrimal system, changes

congenital   Q10.6

canthus, acquired- see Disorder, eyelid, specified type NEC

capillary(acquired)   I78.8

cardiovascular system, congenital   Q28.9

caruncle, lacrimal(acquired) - see also Disorder, lacrimal system, changes

congenital   Q10.6

cascade, stomach   K31.2

cecum(congenital)   Q43.9

acquired   K63.89

cerebral, acquired   G93.89

congenital   Q04.9

cervix (uterus) (acquired) NEC   N88.8

congenital   Q51.9

cheek(acquired)   M95.2

congenital   Q18.9

chest(acquired) (wall)   M95.4

congenital   Q67.8

sequelae (late effect) of rickets   E64.3

chin(acquired)   M95.2

congenital   Q18.9

choroid(congenital)   Q14.3

acquired   H31.8

plexus   Q07.8

acquired   G96.198

cicatricial- see Cicatrix

cilia, acquired- see Disorder, eyelid, specified type NEC

clavicle(acquired)   M95.8

congenital   Q68.8

clitoris(congenital)   Q52.6

acquired   N90.89

clubfoot- see Clubfoot

coccyx(acquired) - see subcategory M43.8

colon(congenital)   Q43.9

acquired   K63.89

concha (ear), congenital - see also Malformation, ear, external

acquired- see Disorder, pinna, deformity

cornea(acquired)   H18.70

congenital   Q13.4

descemetocele- see Descemetocele

ectasia- see Ectasia, cornea

specified NEC   H18.79-

staphyloma- see Staphyloma, cornea

coronary artery(acquired)   I25.9

congenital   Q24.5

cranium(acquired) - see Deformity, skull

cricoid cartilage(congenital)   Q31.8

acquired   J38.7

cystic duct(congenital)   Q44.5

acquired   K82.8

Dandy-Walker   Q03.1

with spina bifida- see Spina bifida

diaphragm(congenital)   Q79.1

acquired   J98.6

digestive organ NOS   Q45.9

ductus arteriosus   Q25.0

duodenal bulb   K31.89

duodenum(congenital)   Q43.9

acquired   K31.89

dura- see Deformity, meninges

ear(acquired) - see also Disorder, pinna, deformity

congenital(external)   Q17.9

internal   Q16.5

middle   Q16.4

ossicles   Q16.3

ossicles   Q16.3

ectodermal (congenital) NEC   Q84.9

ejaculatory duct(congenital)   Q55.4

acquired   N50.89

elbow(joint) (acquired) - see also Deformity, limb, upper arm

congenital   Q68.8

contraction- see Contraction, joint, elbow

endocrine gland NEC   Q89.2

epididymis(congenital)   Q55.4

acquired   N50.89

epiglottis(congenital)   Q31.8

acquired   J38.7

esophagus(congenital)   Q39.9

acquired   K22.89

eustachian tube (congenital) NEC   Q17.8

eye, congenital   Q15.9

eyebrow(congenital)   Q18.8

eyelid(acquired) - see also Disorder, eyelid, specified type NEC

congenital   Q10.3

face(acquired)   M95.2

congenital   Q18.9

fallopian tube, acquired   N83.8

femur(acquired) - see Deformity, limb, specified type NEC, thigh

fetal

with fetopelvic disproportion   O33.7

causing obstructed labor   O66.3

finger(acquired)   M20.00-

boutonniere   M20.02-

congenital   Q68.1

flexion contracture- see Contraction, joint, hand

mallet finger   M20.01-

specified NEC   M20.09-

swan-neck   M20.03-

flexion(joint) (acquired) - see also Deformity, limb, flexion   M21.20

congenital NOS   Q74.9

hip   Q65.89

foot(acquired) - see also Deformity, limb, lower leg

cavovarus(congenital)   Q66.1-

congenital NOS   Q66.9-

specified type NEC   Q66.89

specified type NEC- see Deformity, limb, foot, specified NEC

valgus(congenital)   Q66.6

acquired- see Deformity, valgus, ankle

varus (congenital) NEC   Q66.3-

acquired- see Deformity, varus, ankle

forearm(acquired) - see also Deformity, limb, forearm

congenital   Q68.8

forehead(acquired)   M95.2

congenital   Q75.8

frontal bone(acquired)   M95.2

congenital   Q75.8

gallbladder(congenital)   Q44.1

acquired   K82.8

gastrointestinal tract (congenital) NOS   Q45.9

acquired   K63.89

genitalia, genital organ(s) or system NEC

female(congenital)   Q52.9

acquired   N94.89

external   Q52.70

male(congenital)   Q55.9

acquired   N50.89

globe(eye) (congenital)   Q15.8

acquired   H44.89

gum, acquired NEC   K06.8

hand(acquired) - see Deformity, limb, hand

congenital   Q68.1

head(acquired)   M95.2

congenital   Q75.8

heart(congenital)   Q24.9

septum   Q21.9

auricular - see also Defect, atrial septal   Q21.10

ventricular   Q21.0

valve (congenital) NEC   Q24.8

acquired- see Endocarditis

heel(acquired) - see Deformity, foot

hepatic duct(congenital)   Q44.5

acquired   K83.8

hip(joint) (acquired) - see also Deformity, limb, thigh

congenital   Q65.9

due to (previous) juvenile osteochondrosis- see Coxa, plana

flexion- see Contraction, joint, hip

hourglass- see Contraction, hourglass

humerus(acquired)   M21.82-

congenital   Q74.0

hypophyseal(congenital)   Q89.2

ileocecal(coil) (valve) (acquired)   K63.89

congenital   Q43.9

ileum(congenital)   Q43.9

acquired   K63.89

ilium(acquired)   M95.5

congenital   Q74.2

integument(congenital)   Q84.9

intervertebral cartilage or disc(acquired) - see Disorder, disc, specified NEC

intestine (large) (small) (congenital) NOS   Q43.9

acquired   K63.89

intrinsic minus or plus(hand) - see Deformity, limb, specified type NEC, forearm

iris(acquired)   H21.89

congenital   Q13.2

ischium(acquired)   M95.5

congenital   Q74.2

jaw(acquired) (congenital)   M26.9

joint (acquired) NEC   M21.90

congenital   Q68.8

elbow   M21.92-

hand   M21.94-

hip   M21.95-

knee   M21.96-

shoulder   M21.92-

wrist   M21.93-

kidney(s) (calyx) (pelvis) (congenital)   Q63.9

acquired   N28.89

artery(congenital)   Q27.2

acquired   I77.89

Klippel-Feil(brevicollis)   Q76.1

knee (acquired) NEC - see also Deformity, limb, lower leg

congenital   Q68.2

labium(majus) (minus) (congenital)   Q52.79

acquired   N90.89

lacrimal passages or duct (congenital) NEC   Q10.6

acquired- see Disorder, lacrimal system, changes

larynx(muscle) (congenital)   Q31.8

acquired   J38.7

web(glottic)   Q31.0

leg (upper) (acquired) NEC - see also Deformity, limb, thigh

congenital   Q68.8

lower leg- see Deformity, limb, lower leg

lens(acquired)   H27.8

congenital   Q12.9

lid(fold) (acquired) - see also Disorder, eyelid, specified type NEC

congenital   Q10.3

ligament(acquired) - see Disorder, ligament

congenital   Q79.9

limb(acquired)   M21.90

clawfoot   M21.53-

clawhand   M21.51-

congenital   Q68.1

clubfoot   M21.54-

clubhand   M21.52-

congenital, except reduction deformity   Q74.9

flat foot   M21.4-

flexion   M21.20

ankle   M21.27-

elbow   M21.22-

finger   M21.24-

hip   M21.25-

knee   M21.26-

shoulder   M21.21-

toe   M21.27-

wrist   M21.23-

foot

claw- see Deformity, limb, clawfoot

club- see Deformity, limb, clubfoot

drop   M21.37-

flat- see Deformity, limb, flat foot

specified NEC   M21.6X-

forearm   M21.93-

hand   M21.94-

lower leg   M21.96-

specified type NEC   M21.80

forearm   M21.83-

lower leg   M21.86-

thigh   M21.85-

upper arm   M21.82-

thigh   M21.95-

unequal length   M21.70

short site is

femur   M21.75-

fibula   M21.76-

humerus   M21.72-

radius   M21.73-

tibia   M21.76-

ulna   M21.73-

upper arm   M21.92-

valgus- see Deformity, valgus

varus- see Deformity, varus

wrist drop   M21.33-

lip (acquired) NEC   K13.0

congenital   Q38.0

liver(congenital)   Q44.7

acquired   K76.89

lumbosacral(congenital) (joint) (region)   Q76.49

acquired- see subcategory M43.8

kyphosis- see Kyphosis, congenital

lordosis- see Lordosis, congenital

lung(congenital)   Q33.9

acquired   J98.4

lymphatic system, congenital   Q89.9

Madelung's(radius)   Q74.0

mandible(acquired) (congenital)   M26.9

maxilla(acquired) (congenital)   M26.9

meninges or membrane(congenital)   Q07.9

cerebral   Q04.8

acquired   G96.198

spinal cord(congenital)   Q06.-

acquired   G96.198

metacarpus(acquired) - see Deformity, limb, forearm

congenital   Q74.0

metatarsus(acquired) - see Deformity, foot

congenital   Q66.9-

middle ear(congenital)   Q16.4

ossicles   Q16.3

mitral(leaflets) (valve)   I05.8

parachute   Q23.2

stenosis, congenital   Q23.2

mouth(acquired)   K13.79

congenital   Q38.6

multiple, congenital NEC   Q89.7

muscle(acquired)   M62.89

congenital   Q79.9

sternocleidomastoid   Q68.0

musculoskeletal system(acquired)   M95.9

congenital   Q79.9

specified NEC   M95.8

nail(acquired)   L60.8

congenital   Q84.6

nasal- see Deformity, nose

neck(acquired)   M95.3

congenital   Q18.9

sternocleidomastoid   Q68.0

nervous system(congenital)   Q07.9

nipple(congenital)   Q83.9

acquired   N64.89

nose(acquired) (cartilage)   M95.0

bone(turbinate)   M95.0

congenital   Q30.9

bent or squashed   Q67.4

saddle   M95.0

syphilitic   A50.57

septum(acquired)   J34.2

congenital   Q30.8

sinus(wall) (congenital)   Q30.8

acquired   M95.0

syphilitic(congenital)   A50.57

late   A52.73

ocular muscle(congenital)   Q10.3

acquired- see Strabismus, mechanical

opticociliary vessels(congenital)   Q13.2

orbit(eye) (acquired)   H05.30

atrophy- see Atrophy, orbit

congenital   Q10.7

due to

bone disease NEC   H05.32-

trauma or surgery   H05.33-

enlargement- see Enlargement, orbit

exostosis- see Exostosis, orbit

organ of Corti(congenital)   Q16.5

ovary(congenital)   Q50.39

acquired   N83.8

oviduct, acquired   N83.8

palate(congenital)   Q38.5

acquired   M27.8

cleft(congenital) - see Cleft, palate

pancreas(congenital)   Q45.3

acquired   K86.89

parathyroid(gland)   Q89.2

parotid(gland) (congenital)   Q38.4

acquired   K11.8

patella(acquired) - see Disorder, patella, specified NEC

pelvis, pelvic(acquired) (bony)   M95.5

with disproportion(fetopelvic)   O33.0

causing obstructed labor   O65.0

congenital   Q74.2

rachitic sequelae(late effect)   E64.3

penis(glans) (congenital)   Q55.69

acquired   N48.89

pericardium(congenital)   Q24.8

acquired- see Pericarditis

pharynx(congenital)   Q38.8

acquired   J39.2

pinna, acquired - see also Disorder, pinna, deformity

congenital   Q17.9

pituitary(congenital)   Q89.2

posture- see Dorsopathy, deforming

prepuce(congenital)   Q55.69

acquired   N47.8

prostate(congenital)   Q55.4

acquired   N42.89

pupil(congenital)   Q13.2

acquired- see Abnormality, pupillary

pylorus(congenital)   Q40.3

acquired   K31.89

rachitic (acquired), old or healed   E64.3

radius(acquired) - see also Deformity, limb, forearm

congenital   Q68.8

rectum(congenital)   Q43.9

acquired   K62.89

reduction (extremity) (limb), congenital - see also condition and site   Q73.8

brain   Q04.3

lower- see Defect, reduction, lower limb

upper- see Defect, reduction, upper limb

renal- see Deformity, kidney

respiratory system(congenital)   Q34.9

rib(acquired)   M95.4

congenital   Q76.6

cervical   Q76.5

rotation(joint) (acquired) - see Deformity, limb, specified site NEC

congenital   Q74.9

hip- see Deformity, limb, specified type NEC, thigh

congenital   Q65.89

sacroiliac joint(congenital)   Q74.2

acquired- see subcategory M43.8

sacrum(acquired) - see subcategory M43.8

saddle

back- see Lordosis

nose   M95.0

syphilitic   A50.57

salivary gland or duct(congenital)   Q38.4

acquired   K11.8

scapula(acquired)   M95.8

congenital   Q68.8

scrotum(congenital) - see also Malformation, testis and scrotum

acquired   N50.89

seminal vesicles(congenital)   Q55.4

acquired   N50.89

septum, nasal(acquired)   J34.2

shoulder(joint) (acquired) - see Deformity, limb, upper arm

congenital   Q74.0

contraction- see Contraction, joint, shoulder

sigmoid(flexure) (congenital)   Q43.9

acquired   K63.89

skin(congenital)   Q82.9

skull(acquired)   M95.2

congenital   Q75.8

with

anencephaly   Q00.0

encephalocele- see Encephalocele

hydrocephalus   Q03.9

with spina bifida- see Spina bifida, by site, with hydrocephalus

microcephaly   Q02

soft parts, organs or tissues(of pelvis)

in pregnancy or childbirth NEC   O34.8-

causing obstructed labor   O65.5

spermatic cord(congenital)   Q55.4

acquired   N50.89

torsion- see Torsion, spermatic cord

spinal- see Dorsopathy, deforming

column(acquired) - see Dorsopathy, deforming

congenital   Q67.5

cord(congenital)   Q06.9

acquired   G95.89

nerve root(congenital)   Q07.9

spine(acquired) - see also Dorsopathy, deforming

congenital   Q67.5

rachitic   E64.3

specified NEC- see Dorsopathy, deforming, specified NEC

spleen

acquired   D73.89

congenital   Q89.09

Sprengel's(congenital)   Q74.0

sternocleidomastoid (muscle), congenital   Q68.0

sternum(acquired)   M95.4

congenital NEC   Q76.7

stomach(congenital)   Q40.3

acquired   K31.89

submandibular gland(congenital)   Q38.4

submaxillary gland(congenital)   Q38.4

acquired   K11.8

talipes- see Talipes

testis(congenital) - see also Malformation, testis and scrotum

acquired   N44.8

torsion- see Torsion, testis

thigh(acquired) - see also Deformity, limb, thigh

congenital NEC   Q68.8

thorax(acquired) (wall)   M95.4

congenital   Q67.8

sequelae of rickets   E64.3

thumb(acquired) - see also Deformity, finger

congenital NEC   Q68.1

thymus(tissue) (congenital)   Q89.2

thyroid(gland) (congenital)   Q89.2

cartilage   Q31.8

acquired   J38.7

tibia(acquired) - see also Deformity, limb, specified type NEC, lower leg

congenital NEC   Q68.8

saber(syphilitic)   A50.56

toe(acquired)   M20.6-

congenital   Q66.9-

hallux rigidus   M20.2-

hallux valgus   M20.1-

hallux varus   M20.3-

hammer toe   M20.4-

specified NEC   M20.5X-

tongue(congenital)   Q38.3

acquired   K14.8

tooth, teeth   K00.2

trachea(rings) (congenital)   Q32.1

acquired   J39.8

transverse aortic arch(congenital)   Q25.49

tricuspid(leaflets) (valve)   I07.8

atresia or stenosis   Q22.4

Ebstein's   Q22.5

trunk(acquired)   M95.8

congenital   Q89.9

ulna(acquired) - see also Deformity, limb, forearm

congenital NEC   Q68.8

urachus, congenital   Q64.4

ureter(opening) (congenital)   Q62.8

acquired   N28.89

urethra(congenital)   Q64.79

acquired   N36.8

urinary tract(congenital)   Q64.9

urachus   Q64.4

uterus(congenital)   Q51.9

acquired   N85.8

uvula(congenital)   Q38.5

vagina(acquired)   N89.8

congenital   Q52.4

valgus NEC   M21.00

ankle   M21.07-

elbow   M21.02-

hip   M21.05-

knee   M21.06-

valve, valvular(congenital) (heart)   Q24.8

acquired- see Endocarditis

varus NEC   M21.10

ankle   M21.17-

elbow   M21.12-

hip   M21.15

knee   M21.16-

tibia- see Osteochondrosis, juvenile, tibia

vas deferens(congenital)   Q55.4

acquired   N50.89

vein(congenital)   Q27.9

great   Q26.9

vertebra- see Dorsopathy, deforming

vertical talus(congenital)   Q66.80

left foot   Q66.82

right foot   Q66.81

vesicourethral orifice(acquired)   N32.89

congenital NEC   Q64.79

vessels of optic papilla(congenital)   Q14.2

visual field(contraction) - see Defect, visual field

vitreous body, acquired   H43.89

vulva(congenital)   Q52.79

acquired   N90.89

wrist(joint) (acquired) - see also Deformity, limb, forearm

congenital   Q68.8

contraction- see Contraction, joint, wrist

Degeneration, degenerative

adrenal(capsule) (fatty) (gland) (hyaline) (infectional)   E27.8

amyloid - see also Amyloidosis   E85.9

anterior cornua, spinal cord   G12.29

anterior labral   S43.49-

aorta, aortic   I70.0

fatty   I77.89

aortic valve(heart) - see Endocarditis, aortic

arteriovascular- see Arteriosclerosis

artery, arterial(atheromatous) (calcareous) - see also Arteriosclerosis

cerebral, amyloid   E85.4  [I68.0]

medial- see Arteriosclerosis, extremities

articular cartilage NEC- see Derangement, joint, articular cartilage, by site

atheromatous- see Arteriosclerosis

basal nuclei or ganglia   G23.9

specified NEC   G23.8

bone NEC- see Disorder, bone, specified type NEC

brachial plexus   G54.0

brain(cortical) (progressive)   G31.9

alcoholic   G31.2

arteriosclerotic   I67.2

childhood   G31.9

specified NEC   G31.89

cystic   G31.89

congenital   Q04.6

in

alcoholism   G31.2

beriberi   E51.2

cerebrovascular disease   I67.9

congenital hydrocephalus   Q03.9

with spina bifida - see also Spina bifida

Fabry-Anderson disease   E75.21

Gaucher's disease   E75.22

Hunter's syndrome   E76.1

lipidosis

cerebral   E75.4

generalized   E75.6

mucopolysaccharidosis- see Mucopolysaccharidosis

myxedema   E03.9  [G32.89]

neoplastic disease - see also Neoplasm   D49.6  [G32.89]

Niemann-Pick disease   E75.249  [G32.89]

sphingolipidosis   E75.3  [G32.89]

vitamin B12 deficiency   E53.8  [G32.89]

senile NEC   G31.1

breast   N64.89

Bruch's membrane- see Degeneration, choroid

capillaries(fatty)   I78.8

amyloid   E85.89  [I79.8]

cardiac - see also Degeneration, myocardial

valve, valvular- see Endocarditis

cardiorenal- see Hypertension, cardiorenal

cardiovascular - see also Disease, cardiovascular

renal- see Hypertension, cardiorenal

cerebellar NOS   G31.9

alcoholic   G31.2

primary(hereditary) (sporadic)   G11.9

cerebral- see Degeneration, brain

cerebrovascular   I67.9

due to hypertension   I67.4

cervical plexus   G54.2

cervix   N88.8

due to radiation(intended effect)   N88.8

adverse effect or misadventure   N99.89

chamber angle   H21.21-

changes, spine or vertebra- see Spondylosis

chorioretinal - see also Degeneration, choroid

hereditary   H31.20

choroid(colloid) (drusen)   H31.10-

atrophy- see Atrophy, choroidal

hereditary- see Dystrophy, choroidal, hereditary

ciliary body   H21.22-

cochlear- see subcategory H83.8

combined(spinal cord) (subacute)   E53.8  [G32.0]

with anemia(pernicious)   D51.0  [G32.0]

due to dietary vitamin B12 deficiency   D51.3  [G32.0]

in(due to)

vitamin B12 deficiency   E53.8  [G32.0]

anemia   D51.9  [G32.0]

conjunctiva   H11.10

concretions- see Concretion, conjunctiva

deposits- see Deposit, conjunctiva

pigmentations- see Pigmentation, conjunctiva

pinguecula- see Pinguecula

xerosis- see Xerosis, conjunctiva

cornea   H18.40

calcerous   H18.43

band keratopathy   H18.42-

familial, hereditary- see Dystrophy, cornea

hyaline(of old scars)   H18.49

keratomalacia- see Keratomalacia

nodular   H18.45-

peripheral   H18.46-

senile   H18.41-

specified type NEC   H18.49

cortical(cerebellar) (parenchymatous)   G31.89

alcoholic   G31.2

diffuse, due to arteriopathy   I67.2

corticobasal   G31.85

cutis   L98.8

amyloid   E85.4  [L99]

dental pulp   K04.2

disc disease- see Degeneration, intervertebral disc, by site

dorsolateral(spinal cord) - see Degeneration, combined

extrapyramidal   G25.9

eye, macular - see also Degeneration, macula

congenital or hereditary- see Dystrophy, retina

facet joints- see Spondylosis

fatty

liver NEC   K76.0

alcoholic   K70.0

grey matter(brain) (Alpers')   G31.81

heart - see also Degeneration, myocardial

amyloid   E85.4  [I43]

atheromatous- see Disease, heart, ischemic, atherosclerotic

ischemic- see Disease, heart, ischemic

hepatolenticular(Wilson's)   E83.01

hepatorenal   K76.7

hyaline(diffuse) (generalized)

localized- see Degeneration, by site

infrapatellar fat pad   M79.4

intervertebral disc NOS

with

myelopathy- see Disorder, disc, with, myelopathy

radiculitis or radiculopathy- see Disorder, disc, with, radiculopathy

cervical, cervicothoracic- see Disorder, disc, cervical, degeneration

with

myelopathy- see Disorder, disc, cervical, with myelopathy

neuritis, radiculitis or radiculopathy- see Disorder, disc, cervical, with neuritis

lumbar region   M51.36

with

myelopathy   M51.06

neuritis, radiculitis, radiculopathy or sciatica   M51.16

lumbosacral region   M51.37

with

neuritis, radiculitis, radiculopathy or sciatica   M51.17

sacrococcygeal region   M53.3

thoracic region   M51.34

with

myelopathy   M51.04

neuritis, radiculitis, radiculopathy   M51.14

thoracolumbar region   M51.35

with

myelopathy   M51.05

neuritis, radiculitis, radiculopathy   M51.15

intestine, amyloid   E85.4

iris(pigmentary)   H21.23-

ischemic- see Ischemia

joint disease- see Osteoarthritis

kidney   N28.89

amyloid   E85.4  [N29]

cystic, congenital   Q61.9

fatty   N28.89

polycystic   Q61.3

adult type(autosomal dominant)   Q61.2

infantile type (autosomal recessive) NEC   Q61.19

collecting duct dilatation   Q61.11

Kuhnt-Junius - see also Degeneration, macula   H35.32-

lens- see Cataract

lenticular(familial) (progressive) (Wilson's) (with cirrhosis of liver)   E83.01

liver (diffuse) NEC   K76.89

amyloid   E85.4  [K77]

cystic   K76.89

congenital   Q44.6

fatty NEC   K76.0

alcoholic   K70.0

hypertrophic   K76.89

parenchymatous, acute or subacute   K72.00

with coma   K72.01

pigmentary   K76.89

toxic(acute)   K71.9

lung   J98.4

lymph gland   I89.8

hyaline   I89.8

macula, macular(acquired) (age-related) (senile)   H35.30

angioid streaks   H35.33

atrophic age-related   H35.31-

congenital or hereditary- see Dystrophy, retina

cystoid   H35.35-

drusen   H35.36-

dry age-related   H35.31-

exudative   H35.32-

hole   H35.34-

nonexudative   H35.31-

puckering   H35.37-

toxic   H35.38-

wet age-related   H35.32-

membranous labyrinth, congenital(causing impairment of hearing)   Q16.5

meniscus- see Derangement, meniscus

mitral- see Insufficiency, mitral

Mönckeberg's- see Arteriosclerosis, extremities

motor centers, senile   G31.1

multi-system   G90.3

mural- see Degeneration, myocardial

muscle(fatty) (fibrous) (hyaline) (progressive)   M62.89

heart- see Degeneration, myocardial

myelin, central nervous system   G37.9

myocardial, myocardium(fatty) (hyaline) (senile)   I51.5

with rheumatic fever(conditions in I00)   I09.0

active, acute or subacute   I01.2

with chorea   I02.0

inactive or quiescent(with chorea)   I09.0

hypertensive- see Hypertension, heart

rheumatic- see Degeneration, myocardial, with rheumatic fever

syphilitic   A52.06

nasal sinus(mucosa)   J32.9

frontal   J32.1

maxillary   J32.0

nerve- see Disorder, nerve

nervous system   G31.9

alcoholic   G31.2

amyloid   E85.4  [G99.8]

autonomic   G90.9

fatty   G31.89

specified NEC   G31.89

nipple   N64.89

olivopontocerebellar(hereditary) (familial)   G23.8

osseous labyrinth- see subcategory H83.8

ovary   N83.8

cystic   N83.20-

microcystic   N83.20-

pallidal pigmentary(progressive)   G23.0

pancreas   K86.89

tuberculous   A18.83

penis   N48.89

pigmentary(diffuse) (general)

localized- see Degeneration, by site

pallidal(progressive)   G23.0

pineal gland   E34.8

pituitary(gland)   E23.6

popliteal fat pad   M79.4

posterolateral(spinal cord) - see Degeneration, combined

pulmonary valve(heart)   I37.8

pulp(tooth)   K04.2

pupillary margin   H21.24-

renal- see Degeneration, kidney

retina   H35.9

hereditary(cerebroretinal) (congenital) (juvenile) (macula) (peripheral) (pigmentary) - see Dystrophy, retina

Kuhnt-Junius - see also Degeneration, macula   H35.32-

macula(cystic) (exudative) (hole) (nonexudative) (pseudohole) (senile) (toxic) - see Degeneration, macula

peripheral   H35.40

lattice   H35.41-

microcystoid   H35.42-

paving stone   H35.43-

secondary

pigmentary   H35.45-

vitreoretinal   H35.46-

senile reticular   H35.44-

pigmentary(primary) - see also Dystrophy, retina

secondary- see Degeneration, retina, peripheral, secondary

posterior pole- see Degeneration, macula

saccule, congenital(causing impairment of hearing)   Q16.5

senile   R54

brain   G31.1

cardiac, heart or myocardium- see Degeneration, myocardial

motor centers   G31.1

vascular- see Arteriosclerosis

sinus(cystic) - see also Sinusitis

polypoid   J33.1

skin   L98.8

amyloid   E85.4  [L99]

colloid   L98.8

spinal(cord)   G31.89

amyloid   E85.4  [G32.89]

combined(subacute) - see Degeneration, combined

dorsolateral- see Degeneration, combined

familial NEC   G31.89

fatty   G31.89

funicular- see Degeneration, combined

posterolateral- see Degeneration, combined

subacute combined- see Degeneration, combined

tuberculous   A17.81

spleen   D73.0

amyloid   E85.4  [D77]

stomach   K31.89

striatonigral   G23.2

suprarenal(capsule) (gland)   E27.8

synovial membrane(pulpy) - see Disorder, synovium, specified type NEC

tapetoretinal- see Dystrophy, retina

thymus(gland)   E32.8

fatty   E32.8

thyroid(gland)   E07.89

tricuspid(heart) (valve)   I07.9

tuberculous NEC- see Tuberculosis

turbinate   J34.89

uterus(cystic)   N85.8

vascular(senile) - see Arteriosclerosis

hypertensive- see Hypertension

vitreoretinal, secondary- see Degeneration, retina, peripheral, secondary, vitreoretinal

vitreous(body)   H43.81-

Wallerian- see Disorder, nerve

Wilson's hepatolenticular   E83.01

Deglutition

paralysis   R13.0

hysterical   F44.4

pneumonia   J69.0

Degos' disease   I77.89

Dehiscence(of)

amputation stump   T87.81

cesarean wound   O90.0

closure of

cornea   T81.31

craniotomy   T81.32

fascia(muscular) (superficial)   T81.32

internal organ or tissue   T81.32

laceration(external) (internal)   T81.33

ligament   T81.32

mucosa   T81.31

muscle or muscle flap   T81.32

ribs or rib cage   T81.32

skin and subcutaneous tissue(full-thickness) (superficial)   T81.31

skull   T81.32

sternum(sternotomy)   T81.32

tendon   T81.32

traumatic laceration(external) (internal)   T81.33

episiotomy   O90.1

operation wound NEC   T81.31

external operation wound(superficial)   T81.31

internal operation wound(deep)   T81.32

perineal wound(postpartum)   O90.1

traumatic injury wound repair   T81.33

wound   T81.30

traumatic repair   T81.33

Dehydration   E86.0

newborn   P74.1

Déjérine-Roussy syndrome   G89.0

Déjérine-Sottas disease or neuropathy(hypertrophic)   G60.0

Déjérine-Thomas atrophy   G23.8

Delay, delayed

any plane in pelvis

complicating delivery   O66.9

birth or delivery NOS   O63.9

closure, ductus arteriosus(Botalli)   P29.38

coagulation- see Defect, coagulation

conduction(cardiac) (ventricular)   I45.9

delivery, second twin, triplet, etc   O63.2

development   R62.50

global   F88

intellectual(specific)   F81.9

language   F80.9

due to hearing loss   F80.4

learning   F81.9

milestone   R62.0

pervasive   F84.9

physiological   R62.50

specified stage NEC   R62.0

reading   F81.0

sexual   E30.0

speech   F80.9

due to hearing loss   F80.4

spelling   F81.81

ejaculation   F52.32

gastric emptying   K30

menarche   E30.0

menstruation(cause unknown)   N91.0

milestone   R62.0

passage of meconium(newborn)   P76.0

primary respiration   P28.9

puberty(constitutional)   E30.0

separation of umbilical cord   P96.82

sexual maturation, female   E30.0

sleep phase syndrome   G47.21

union, fracture- see Fracture, by site

vaccination   Z28.9

Deletion(s)

autosome   Q93.9

identified by fluorescence in situ hybridization(FISH)   Q93.89

identified by in situ hybridization(ISH)   Q93.89

chromosome

with complex rearrangements NEC   Q93.7

part of NEC   Q93.59

seen only at prometaphase   Q93.89

short arm

4   Q93.3

5p   Q93.4

22q11.2   Q93.81

specified NEC   Q93.89

long arm chromosome 18 or 21   Q93.89

with complex rearrangements NEC   Q93.7

microdeletions NEC   Q93.88

Delhi boil or button   B55.1

Delinquency(juvenile) (neurotic)   F91.8

group   Z72.810

Delinquent immunization status   Z28.39

COVID-19   Z28.31-

Delirium, delirious(acute or subacute) (not alcohol- or drug-induced) (with dementia)   R41.0

alcoholic(acute) (tremens) (withdrawal)   F10.921

with intoxication   F10.921

in

abuse   F10.121

dependence   F10.221

due to(secondary to)

alcohol

intoxication   F10.921

in

abuse   F10.121

dependence   F10.221

withdrawal   F10.231

amphetamine intoxication   F15.921

in

abuse   F15.121

dependence   F15.221

anxiolytic

intoxication   F13.921

in

abuse   F13.121

dependence   F13.221

withdrawal   F13.231

cannabis intoxication(acute)   F12.921

in

abuse   F12.121

dependence   F12.221

cocaine intoxication(acute)   F14.921

in

abuse   F14.121

dependence   F14.221

general medical condition   F05

hallucinogen intoxication   F16.921

in

abuse   F16.121

dependence   F16.221

hypnotic

intoxication   F13.921

in

abuse   F13.121

dependence   F13.221

withdrawal   F13.231

inhalant intoxication(acute)   F18.921

in

abuse   F18.121

dependence   F18.221

multiple etiologies   F05

opioid intoxication(acute)   F11.921

in

abuse   F11.121

dependence   F11.221

other (or unknown) substance   F19.921

phencyclidine intoxication(acute)   F16.921

in

abuse   F16.121

dependence   F16.221

psychoactive substance NEC intoxication(acute)   F19.921

in

abuse   F19.121

dependence   F19.221

sedative

intoxication   F13.921

in

abuse   F13.121

dependence   F13.221

withdrawal   F13.231

unknown etiology   R41.0

exhaustion   F43.0

hysterical   F44.89

postprocedural(postoperative)   F05

puerperal   F05

thyroid- see Thyrotoxicosis with thyroid storm

traumatic- see Injury, intracranial

tremens(alcohol-induced)   F10.231

sedative-induced   F13.231

Delivery(childbirth) (labor)

arrested active phase   O62.1

cesarean(for)

abnormal

pelvis(bony) (deformity) (major) NEC with disproportion (fetopelvic)   O33.0

with obstructed labor   O65.0

presentation or position   O32.9

abruptio placentae - see also Abruptio placentae   O45.9-

acromion presentation   O32.2

atony, uterus   O62.2

breech presentation   O32.1

incomplete   O32.8

brow presentation   O32.3

cephalopelvic disproportion   O33.9

cerclage   O34.3-

chin presentation   O32.3

cicatrix of cervix   O34.4-

contracted pelvis(general)

inlet   O33.2

outlet   O33.3

cord presentation or prolapse   O69.0

cystocele   O34.8-

deformity(acquired) (congenital)

pelvic organs or tissues NEC   O34.8-

pelvis (bony) NEC   O33.0

disproportion NOS   O33.9

eclampsia- see Eclampsia

face presentation   O32.3

failed

forceps   O66.5

induction of labor   O61.9

instrumental   O61.1

mechanical   O61.1

medical   O61.0

specified NEC   O61.8

surgical   O61.1

trial of labor NOS   O66.40

following previous cesarean delivery   O66.41

vacuum extraction   O66.5

ventouse   O66.5

fetal-maternal hemorrhage   O43.01-

hemorrhage(intrapartum)   O67.9

with coagulation defect   O67.0

specified cause NEC   O67.8

high head at term   O32.4

hydrocephalic fetus   O33.6

incarceration of uterus   O34.51-

incoordinate uterine action   O62.4

increased size, fetus   O33.5

inertia, uterus   O62.2

primary   O62.0

secondary   O62.1

isthmocele   O34.22

lateroversion, uterus   O34.59-

mal lie   O32.9

malposition

fetus   O32.9

pelvic organs or tissues NEC   O34.8-

uterus NEC   O34.59-

malpresentation NOS   O32.9

oblique presentation   O32.2

occurring after 37 completed weeks of gestation but before 39 completed weeks gestation due to (spontaneous) onset of labor   O75.82

oversize fetus   O33.5

pelvic tumor NEC   O34.8-

placenta previa   O44.0-

complete   O44.0-

with hemorrhage   O44.1-

placental insufficiency   O36.51-

planned, occurring after 37 completed weeks of gestation but before 39 completed weeks gestation due to (spontaneous) onset of labor   O75.82

polyp, cervix   O34.4-

causing obstructed labor   O65.5

poor dilatation, cervix   O62.0

pre-eclampsia   O14.94

mild   O14.04

moderate   O14.04

severe   O14.14

with hemolysis, elevated liver enzymes and low platelet count(HELLP)   O14.24

previous

cesarean delivery   O34.219

classical (vertical) scar   O34.212

isthmocele   O34.22

low transverse scar   O34.211

mid-transverse T incision   O34.218

scar

defect(isthmocele)   O34.22

specified type NEC   O34.218

surgery(to)

cervix   O34.4-

gynecological NEC   O34.8-

rectum   O34.7-

uterus   O34.29

vagina   O34.6-

prolapse

arm or hand   O32.2

uterus   O34.52-

prolonged labor NOS   O63.9

rectocele   O34.8-

retroversion

uterus   O34.53-

rigid

cervix   O34.4-

pelvic floor   O34.8-

perineum   O34.7-

vagina   O34.6-

vulva   O34.7-

sacculation, pregnant uterus   O34.59-

scar(s)

cervix   O34.4-

cesarean delivery   O34.219

classical(vertical)   O34.212

isthmocele   O34.22

low transverse   O34.211

mid-transverse T incision   O34.218

scar

defect(isthmocele)   O34.22

specified type NEC   O34.218

defect(isthmocele)   O34.22

transmural uterine   O34.29

uterus   O34.29

Shirodkar suture in situ   O34.3-

shoulder presentation   O32.2

stenosis or stricture, cervix   O34.4-

streptococcus group B (GBS) carrier state   O99.824

transmural uterine scar   O34.29

transverse presentation or lie   O32.2

tumor, pelvic organs or tissues NEC   O34.8-

cervix   O34.4-

umbilical cord presentation or prolapse   O69.0

without indication   O82

completely normal case   O80

complicated   O75.9

by

abnormal, abnormality(of)

forces of labor   O62.9

specified type NEC   O62.8

glucose   O99.814

uterine contractions NOS   O62.9

abruptio placentae - see also Abruptio placentae   O45.9-

abuse

physical   O9A.32

psychological   O9A.52

sexual   O9A.42

adherent placenta   O72.0

without hemorrhage   O73.0

alcohol use   O99.314

anemia(pre-existing)   O99.02

anesthetic death   O74.8

annular detachment of cervix   O71.3

atony, uterus   O62.2

attempted vacuum extraction and forceps   O66.5

Bandl's ring   O62.4

bariatric surgery status   O99.844

biliary tract disorder   O26.62

bleeding- see Delivery, complicated by, hemorrhage

blood disorder NEC   O99.12

cervical dystocia(hypotonic)   O62.2

primary   O62.0

secondary   O62.1

circulatory system disorder   O99.42

compression of cord (umbilical) NEC   O69.2

condition NEC   O99.892

contraction, contracted ring   O62.4

cord(umbilical)

around neck

with compression   O69.1

without compression   O69.81

bruising   O69.5

complication   O69.9

specified NEC   O69.89

compression NEC   O69.2

entanglement   O69.2

without compression   O69.82

hematoma   O69.5

presentation   O69.0

prolapse   O69.0

short   O69.3

thrombosis(vessels)   O69.5

vascular lesion   O69.5

Couvelaire uterus   O45.8X-

damage to (injury to) NEC

perineum   O71.82

periurethral tissue   O71.82

vulva   O71.82

delay following rupture of membranes(spontaneous) - see Pregnancy, complicated by, premature rupture of membranes

depressed fetal heart tones   O76

diabetes   O24.92

gestational   O24.429

diet controlled   O24.420

insulin controlled   O24.424

oral drug controlled(antidiabetic) (hypoglycemic)   O24.425

pre-existing   O24.32

specified NEC   O24.82

type 1   O24.02

type 2   O24.12

diastasis recti(abdominis)   O71.89

dilatation

bladder   O66.8

cervix incomplete, poor or slow   O62.0

disease NEC   O99.892

disruptio uteri- see Delivery, complicated by, rupture, uterus

drug use   O99.324

dysfunction, uterus NOS   O62.9

hypertonic   O62.4

hypotonic   O62.2

primary   O62.0

secondary   O62.1

incoordinate   O62.4

eclampsia   O15.1

embolism(pulmonary) - see Embolism, obstetric

endocrine, nutritional or metabolic disease NEC   O99.284

failed

attempted vaginal birth after previous cesarean delivery   O66.41

induction of labor   O61.9

instrumental   O61.1

mechanical   O61.1

medical   O61.0

specified NEC   O61.8

surgical   O61.1

trial of labor   O66.40

female genital mutilation   O65.5

fetal

abnormal acid-base balance   O68

acidemia   O68

acidosis   O68

alkalosis   O68

death, early   O02.1

deformity   O66.3

heart rate or rhythm(abnormal) (non-reassuring)   O76

hypoxia   O77.8

stress   O77.9

due to drug administration   O77.1

electrocardiographic evidence of   O77.8

specified NEC   O77.8

ultrasound evidence of   O77.8

fever during labor   O75.2

gastric banding status   O99.844

gastric bypass status   O99.844

gastrointestinal disease NEC   O99.62

gestational

diabetes   O24.429

diet controlled   O24.420

insulin (and diet) controlled   O24.424

oral drug controlled(antidiabetic) (hypoglycemic)   O24.425

edema   O12.04

with proteinuria   O12.24

proteinuria   O12.14

gonorrhea   O98.22

hematoma   O71.7

ischial spine   O71.7

pelvic   O71.7

vagina   O71.7

vulva or perineum   O71.7

hemorrhage(uterine)   O67.9

associated with

afibrinogenemia   O67.0

coagulation defect   O67.0

hyperfibrinolysis   O67.0

hypofibrinogenemia   O67.0

due to

low implantation of placenta   O44.5-

low lying placenta   O44.5-

placenta previa   O44.1-

marginal   O44.3-

partial   O44.3-

premature separation of placenta(normally implanted) - see also Abruptio placentae   O45.9-

retained placenta   O72.0

uterine leiomyoma   O67.8

placenta NEC   O67.8

postpartum NEC(atonic) (immediate)   O72.1

with retained or trapped placenta   O72.0

delayed   O72.2

secondary   O72.2

third stage   O72.0

hourglass contraction, uterus   O62.4

hypertension, hypertensive(pre-existing) - see Hypertension, complicated by, childbirth (labor)

hypotension   O26.5-

incomplete dilatation(cervix)   O62.0

incoordinate uterus contractions   O62.4

inertia, uterus   O62.2

during latent phase of labor   O62.0

primary   O62.0

secondary   O62.1

infection(maternal)   O98.92

carrier state NEC   O99.834

gonorrhea   O98.22

human immunodeficiency virus(HIV)   O98.72

sexually transmitted NEC   O98.32

specified NEC   O98.82

syphilis   O98.12

tuberculosis   O98.02

viral hepatitis   O98.42

viral NEC   O98.52

injury(to mother) - see also Delivery, complicated, by, damage to   O71.9

nonobstetric   O9A.22

caused by abuse- see Delivery, complicated by, abuse

intrauterine fetal death, early   O02.1

inversion, uterus   O71.2

laceration(perineal)   O70.9

anus(sphincter)   O70.4

with third degree laceration - see also Delivery, complicated, by, laceration, perineum, third degree   O70.20

with mucosa   O70.3

without third degree laceration   O70.4

bladder(urinary)   O71.5

bowel   O71.5

cervix(uteri)   O71.3

fourchette   O70.0

hymen   O70.0

labia   O70.0

pelvic

floor   O70.1

organ NEC   O71.5

perineum, perineal   O70.9

first degree   O70.0

fourth degree   O70.3

muscles   O70.1

second degree   O70.1

skin   O70.0

slight   O70.0

third degree   O70.20

with

both external anal sphincter(EAS) and internal anal sphincter (IAS) torn (IIIc)   O70.23

less than 50% of external anal sphincter (EAS) thickness torn(IIIa)   O70.21

more than 50% external anal sphincter (EAS) thickness torn(IIIb)   O70.22

IIIa   O70.21

IIIb   O70.22

IIIc   O70.23

peritoneum(pelvic)   O71.5

rectovaginal(septum) (without perineal laceration)   O71.4

with perineum - see also Delivery, complicated, by, laceration, perineum, third degree   O70.20

with anal or rectal mucosa   O70.3

specified NEC   O71.89

sphincter ani- see Delivery, complicated, by, laceration, anus (sphincter)

urethra   O71.5

uterus   O71.81

before labor   O71.81

vagina, vaginal(deep) (high) (without perineal laceration)   O71.4

with perineum   O70.0

muscles, with perineum   O70.1

vulva   O70.0

liver disorder   O26.62

malignancy   O9A.12

malnutrition   O25.2

malposition, malpresentation

placenta   O44.0-

with hemorrhage   O44.1-

uterus or cervix   O65.5

without obstruction - see also Delivery, complicated by, obstruction   O32.9

breech   O32.1

compound   O32.6

face(brow) (chin)   O32.3

footling   O32.8

high head   O32.4

oblique   O32.2

specified NEC   O32.8

transverse   O32.2

unstable lie   O32.0

meconium in amniotic fluid   O77.0

mental disorder NEC   O99.344

metrorrhexis- see Delivery, complicated by, rupture, uterus

nervous system disorder   O99.354

obesity(pre-existing)   O99.214

obesity surgery status   O99.844

obstetric trauma   O71.9

specified NEC   O71.89

obstructed labor

due to

breech (complete) (frank) presentation   O64.1

incomplete   O64.8

brow presentation   O64.3

buttock presentation   O64.1

chin presentation   O64.2

compound presentation   O64.5

contracted pelvis   O65.1

deep transverse arrest   O64.0

deformed pelvis   O65.0

dystocia(fetal)   O66.9

due to

conjoined twins   O66.3

fetal

abnormality NEC   O66.3

ascites   O66.3

hydrops   O66.3

meningomyelocele   O66.3

sacral teratoma   O66.3

tumor   O66.3

hydrocephalic fetus   O66.3

shoulder   O66.0

face presentation   O64.2

fetopelvic disproportion   O65.4

footling presentation   O64.8

impacted shoulders   O66.0

incomplete rotation of fetal head   O64.0

large fetus   O66.2

locked twins   O66.1

malposition   O64.9

specified NEC   O64.8

malpresentation   O64.9

specified NEC   O64.8

multiple fetuses NEC   O66.6

pelvic

abnormality(maternal)   O65.9

organ   O65.5

specified NEC   O65.8

contraction

inlet   O65.2

mid-cavity   O65.3

outlet   O65.3

persistent(position)

occipitoiliac   O64.0

occipitoposterior   O64.0

occipitosacral   O64.0

occipitotransverse   O64.0