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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

Angelman syndrome

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

Q93.88 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

Q95 Balanced rearrangements and structural markers, not elsewhere classified

Includes: Robertsonian and balanced reciprocal translocations and insertions

Q95.0 Balanced translocation and insertion in normal individual

Q95.1 Chromosome inversion in normal individual

Q95.2 Balanced autosomal rearrangement in abnormal individual

Q95.3 Balanced sex/autosomal rearrangement in abnormal individual

Q95.5 Individual with autosomal fragile site

Q95.8 Other balanced rearrangements and structural markers

Q95.9 Balanced rearrangement and structural marker, unspecified

Q96 Turner's syndrome

Excludes1: Noonan syndrome (Q87.1)

Q96.0 Karyotype 45, X

Q96.1 Karyotype 46, X iso (Xq)

Karyotype 46, isochromosome Xq

Q96.