Kahler's disease C90.0-
Kakke E51.11
Kala-azar B55.0
Kallmann's syndrome E23.0
Kanner's syndrome(autism) - see Psychosis, childhood
Kaposi's
dermatosis(xeroderma pigmentosum) Q82.1
lichen ruber L44.0
acuminatus L44.0
sarcoma
colon C46.4
connective tissue C46.1
gastrointestinal organ C46.4
lung C46.5-
lymph node(multiple) C46.3
palate(hard) (soft) C46.2
rectum C46.4
skin(multiple sites) C46.0
specified site NEC C46.7
stomach C46.4
unspecified site C46.9
varicelliform eruption B00.0
vaccinia T88.1
Kartagener's syndrome or triad(sinusitis, bronchiectasis, situs inversus) Q89.3
Karyotype
with abnormality except iso(Xq) Q96.2
45,X Q96.0
46,X
iso(Xq) Q96.1
46,XX Q98.3
with streak gonads Q50.32
hermaphrodite(true) Q99.1
male Q98.3
46,XY
with streak gonads Q56.1
female Q97.3
hermaphrodite(true) Q99.1
47,XXX Q97.0
47,XXY Q98.0
47,XYY Q98.5
Kaschin-Beck disease- see Disease, Kaschin-Beck
Katayama's disease or fever B65.2
Kawasaki's syndrome M30.3
Kayser-Fleischer ring(cornea) (pseudosclerosis) H18.04-
Kaznelson's syndrome(congenital hypoplastic anemia) D61.01
Kearns-Sayre syndrome H49.81-
Kedani fever A75.3
Kelis L91.0
Kelly(-Patterson) syndrome(sideropenic dysphagia) D50.1
Keloid, cheloid L91.0
acne L73.0
Addison's L94.0
cornea- see Opacity, cornea
Hawkin's L91.0
scar L91.0
Keloma L91.0
Kenya fever A77.1
Keratectasia - see also Ectasia, cornea
congenital Q13.4
Keratinization of alveolar ridge mucosa
excessive K13.23
minimal K13.22
Keratinized residual ridge mucosa
excessive K13.23
minimal K13.22
Keratitis(nodular) (nonulcerative) (simple) (zonular) H16.9
with ulceration(central) (marginal) (perforated) (ring) - see Ulcer, cornea
actinic- see Photokeratitis
arborescens(herpes simplex) B00.52
areolar H16.11-
bullosa H16.8
deep H16.309
specified type NEC H16.399
dendritic(a) (herpes simplex) B00.52
disciform(is) (herpes simplex) B00.52
varicella B01.81
filamentary H16.12-
gonococcal(congenital or prenatal) A54.33
herpes, herpetic(simplex) B00.52
zoster B02.33
in(due to)
acanthamebiasis B60.13
adenovirus B30.0
exanthema - see also Exanthem B09
herpes (simplex) virus B00.52
measles B05.81
syphilis A50.31
tuberculosis A18.52
zoster B02.33
interstitial(nonsyphilitic) H16.30-
diffuse H16.32-
herpes, herpetic(simplex) B00.52
zoster B02.33
sclerosing H16.33-
specified type NEC H16.39-
syphilitic(congenital) (late) A50.31
tuberculous A18.52
macular H16.11-
nummular H16.11-
oyster shuckers' H16.8
parenchymatous- see Keratitis, interstitial
petrificans H16.8
postmeasles B05.81
punctata
syphilitic(profunda) A50.31
punctate H16.14-
purulent H16.8
rosacea L71.8
sclerosing H16.33-
specified type NEC H16.8
stellate H16.11-
striate H16.11-
superficial H16.10-
with conjunctivitis- see Keratoconjunctivitis
due to light- see Photokeratitis
suppurative H16.8
syphilitic(congenital) (prenatal) A50.31
trachomatous A71.1
sequelae B94.0
tuberculous A18.52
vesicular H16.8
xerotic - see also Keratomalacia H16.8
vitamin A deficiency E50.4
Keratoacanthoma L85.8
Keratocele- see Descemetocele
Keratoconjunctivitis H16.20-
Acanthamoeba B60.13
adenoviral B30.0
epidemic B30.0
exposure H16.21-
herpes, herpetic(simplex) B00.52
zoster B02.33
in exanthema - see also Exanthem B09
infectious B30.0
lagophthalmic- see Keratoconjunctivitis, specified type NEC
neurotrophic H16.23-
phlyctenular H16.25-
postmeasles B05.81
shipyard B30.0
sicca(Sjögren's) M35.0-
not Sjögren's H16.22-
specified type NEC H16.29-
tuberculous(phlyctenular) A18.52
vernal H16.26-
Keratoconus H18.60-
congenital Q13.4
stable H18.61-
unstable H18.62-
Keratocyst(dental) (odontogenic) - see Cyst, calcifying odontogenic
Keratoderma, keratodermia(congenital) (palmaris et plantaris) (symmetrical) Q82.8
acquired L85.1
in diseases classified elsewhere L86
climactericum L85.1
gonococcal A54.89
gonorrheal A54.89
punctata L85.2
Reiter's- see Reiter's disease
Keratodermatocele- see Descemetocele
Keratoglobus H18.79
congenital Q15.8
with glaucoma Q15.0
Keratohemia- see Pigmentation, cornea, stromal
Keratoiritis - see also Iridocyclitis
syphilitic A50.39
tuberculous A18.54
Keratoma L57.0
palmaris and plantaris hereditarium Q82.8
senile L57.0
Keratomalacia H18.44-
vitamin A deficiency E50.4
Keratomegaly Q13.4
Keratomycosis B49
nigrans, nigricans(palmaris) B36.1
Keratopathy H18.9
band H18.42-
bullous H18.1-
bullous (aphakic), following cataract surgery H59.01-
Keratoscleritis, tuberculous A18.52
Keratosis L57.0
actinic L57.0
arsenical L85.8
congenital, specified NEC Q80.8
female genital NEC N94.89
follicularis Q82.8
acquired L11.0
congenita Q82.8
et parafollicularis in cutem penetrans L87.0
spinulosa(decalvans) Q82.8
vitamin A deficiency E50.8
gonococcal A54.89
male genital(external) N50.89
nigricans L83
obturans, external ear(canal) - see Cholesteatoma, external ear
palmaris et plantaris(inherited) (symmetrical) Q82.8
acquired L85.1
penile N48.89
pharynx J39.2
pilaris, acquired L85.8
punctata(palmaris et plantaris) L85.2
scrotal N50.89
seborrheic L82.1
inflamed L82.0
senile L57.0
solar L57.0
tonsillaris J35.8
vagina N89.4
vegetans Q82.8
vitamin A deficiency E50.8
vocal cord J38.3
Kerato-uveitis- see Iridocyclitis
Kerunoparalysis T75.09
Kerion(celsi) B35.0
Kernicterus of newborn(not due to isoimmunization) P57.9
due to isoimmunization(conditions in P55.0-P55.9) P57.0
specified type NEC P57.8
Keshan disease E59
Ketoacidosis E87.29
diabetic- see Diabetes, by type, with ketoacidosis
Ketonuria R82.4
Ketosis NEC E88.89
diabetic- see Diabetes, by type, with ketoacidosis
Kew Garden fever A79.1
Kidney- see condition
Kienböck's disease - see also Osteochondrosis, juvenile, hand, carpal lunate
adult M93.1
Kimmelstiel (-Wilson) disease- see Diabetes, Kimmelstiel (-Wilson) disease
Kimura disease D21.9
specified site(see Neoplasm, connective tissue benign)
Kink, kinking
artery I77.1
hair(acquired) L67.8
ileum or intestine- see Obstruction, intestine
Lane's- see Obstruction, intestine
organ or site, congenital NEC- see Anomaly, by site
ureter(pelvic junction) N13.5
with
hydronephrosis N13.1
with infection N13.6
pyelonephritis(chronic) N11.1
congenital Q62.39
vein(s) I87.8
caval I87.1
peripheral I87.1
Kinnier Wilson's disease(hepatolenticular degeneration) E83.01
Kissing spine M48.20
cervical region M48.22
cervicothoracic region M48.23
lumbar region M48.26
lumbosacral region M48.27
occipito-atlanto-axial region M48.21
thoracic region M48.24
thoracolumbar region M48.25
Klatskin's tumor C24.0
Klauder's disease A26.8
Klebs' disease - see also Glomerulonephritis N05.-
Klebsiella (K.) pneumoniae, as cause of disease classified elsewhere B96.1
Klein (e) -Levin syndrome G47.13
Kleptomania F63.2
Klinefelter's syndrome Q98.4
karyotype 47,XXY Q98.0
male with more than two X chromosomes Q98.1
Klippel-Feil deficiency, disease, or syndrome(brevicollis) Q76.1
Klippel's disease I67.2
Klippel-Trenaunay (-Weber) syndrome Q87.2
Klumpke(-Déjerine) palsy, paralysis (birth) (newborn) P14.1
Knee- see condition
Knock knee(acquired) M21.06-
congenital Q74.1
Knot(s)
intestinal, syndrome(volvulus) K56.2
surfer S89.8-
umbilical cord(true) O69.2
Knotting(of)
hair L67.8
intestine K56.2
Knuckle pad(Garrod's) M72.1
Koch's
infection- see Tuberculosis
relapsing fever A68.9
Koch-Weeks' conjunctivitis- see Conjunctivitis, acute, mucopurulent
Köebner's syndrome Q81.8
Köenig's disease(osteochondritis dissecans) - see Osteochondritis, dissecans
Köhler-Pellegrini-Steida disease or syndrome(calcification, knee joint) - see Bursitis, tibial collateral
Köhler's disease
patellar- see Osteochondrosis, juvenile, patella
tarsal navicular- see Osteochondrosis, juvenile, tarsus
Koilonychia L60.3
congenital Q84.6
Kojevnikov's, epilepsy- see Kozhevnikof's epilepsy
Koplik's spots B05.9
Kopp's asthma E32.8
Korsakoff's (Wernicke) disease, psychosis or syndrome(alcoholic) F10.96
with dependence F10.26
drug-induced
due to drug abuse- see Abuse, drug, by type, with amnestic disorder
due to drug dependence- see Dependence, drug, by type, with amnestic disorder
nonalcoholic F04
Korsakov's disease, psychosis or syndrome- see Korsakoff's disease
Korsakow's disease, psychosis or syndrome- see Korsakoff's disease
Kostmann's disease or syndrome(infantile genetic agranulocytosis) - see Agranulocytosis
Kozhevnikof's epilepsy G40.109
intractable G40.119
with status epilepticus G40.111
without status epilepticus G40.119
not intractable G40.109
with status epilepticus G40.101
without status epilepticus G40.109
Krabbe's
disease E75.23
syndrome, congenital muscle hypoplasia Q79.8
Kraepelin-Morel disease- see Schizophrenia
Kraft-Weber-Dimitri disease Q85.89
Kraurosis
ani K62.89
penis N48.0
vagina N89.8
vulva N90.4
Kreotoxism A05.9
Krukenberg's
spindle- see Pigmentation, cornea, posterior
tumor C79.6-
Kufs' disease E75.4
Kugelberg-Welander disease G12.1
Kuhnt-Junius degeneration - see also Degeneration, macula H35.32-
Kümmell's disease or spondylitis- see Spondylopathy, traumatic
Kupffer cell sarcoma C22.3
Kuru A81.81
Kussmaul's
disease M30.0
respiration E87.29
in diabetic acidosis- see Diabetes, by type, with ketoacidosis
Kwashiorkor E40
marasmic, marasmus type E42
Kyasanur Forest disease A98.2
Kyphoscoliosis, kyphoscoliotic(acquired) - see also Scoliosis M41.9
congenital Q67.5
heart(disease) I27.1
sequelae of rickets E64.3
tuberculous A18.01
Kyphosis, kyphotic(acquired) M40.209
cervical region M40.202
cervicothoracic region M40.203
congenital Q76.419
cervical region Q76.412
cervicothoracic region Q76.413
occipito-atlanto-axial region Q76.411
thoracic region Q76.414
thoracolumbar region Q76.415
Morquio-Brailsford type(spinal) - see also subcategory M49.8 E76.219
postlaminectomy M96.3
postradiation therapy M96.2
postural(adolescent) M40.00
cervicothoracic region M40.03
thoracic region M40.04
thoracolumbar region M40.05
secondary NEC M40.10
cervical region M40.12
cervicothoracic region M40.13
thoracic region M40.14
thoracolumbar region M40.15
sequelae of rickets E64.3
specified type NEC M40.299
cervical region M40.292
cervicothoracic region M40.293
thoracic region M40.294
thoracolumbar region M40.295
syphilitic, congenital A50.56
thoracic region M40.204
thoracolumbar region M40.205
tuberculous A18.01
Kyrle disease L87.0