| ICD-10-CM-2023 > Q00-Q99 > Q90-Q99 > Q93 |
Q90-Q99 | Chromosomal abnormalities, not elsewhere classified | |
Excl2.: | mitochondrial metabolic disorders (E88.4-) | |
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 | |
Info: | Wolff-Hirschorn syndrome | |
Q93.4 | Deletion of short arm of chromosome 5 | |
Info: | Cri-du-chat syndrome | |
Q93.5 | Other deletions of part of a chromosome | |
Q93.51 | Angelman syndrome | |
Q93.59 | Other deletions of part of a chromosome | |
Q93.7 | Deletions with other complex rearrangements | |
Info: | Deletions due to unbalanced translocations, inversions and insertions | |
Use add'l | 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 | |
Info: | Deletion 22q11.2 | |
Q93.82 | Williams syndrome | |
Q93.88 | Other microdeletions | |
Info: | Miller-Dieker syndrome Smith-Magenis syndrome | |
Q93.89 | Other deletions from the autosomes | |
Info: | 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 | |
|
ICD-10-CM-2023 Code Search Engine and PCS-2023 Code Search Engine |