Page:ICD-10-CM (2010).djvu/1141

 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.