Category: Q93 - Monosomies and deletions from the autosomes, not elsewhere classified

 Chapter Notes

 Section Notes

 Q93

Monosomies and deletions from the autosomes, not elsewhere classified

 Q93.0

Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction)

 Q93.1

Whole chromosome monosomy, mosaicism (mitotic nondisjunction)

 Q93.2

Chromosome replaced with ring, dicentric or isochromosome

 Q93.3

Deletion of short arm of chromosome 4

Wolff-Hirschorn syndrome

 Q93.4

Deletion of short arm of chromosome 5

Cri-du-chat syndrome

 Q93.5

Other deletions of part of a chromosome

 Q93.51

Angelman syndrome

 Q93.52

Phelan-McDermid syndrome

22q13.3 deletion syndrome

Use additional code(s) to identify any associated conditions, such as:

autism spectrum disorder (F84.0)

degree of intellectual disabilities (F70-F79)

epilepsy and recurrent seizures (G40.-)

lymphedema (I89.0)

 Q93.59

Other deletions of part of a chromosome

 Q93.7

Deletions with other complex rearrangements

Deletions due to unbalanced translocations, inversions and insertions

Code also any associated duplications due to unbalanced translocations, inversions and insertions (Q92.5)

 Q93.8

Other deletions from the autosomes

 Q93.81

Velo-cardio-facial syndrome

Deletion 22q11.2

 Q93.82

Williams syndrome

 Q93.88

Other microdeletions

Miller-Dieker syndrome

Smith-Magenis syndrome

 Q93.89

Other deletions from the autosomes

Deletions identified by fluorescence in situ hybridization (FISH)

Deletions identified by in situ hybridization (ISH)

Deletions seen only at prometaphase

 Q93.9

Deletion from autosomes, unspecified