ICD-10-CM Q00 to Q99
Congenital malformations, deformations and chromosomal abnormalities: one chapter of ICD-10-CM.
1,055 codes · page 21 of 22 · every chapter
Whole chromosome monosomy,nonmosaic (meiotic nondisjunction) Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction) Q93.0 Whole chromosome monosomy, mosaicism (mitotic nondisjunction) Q93.1 Chromosome replaced with ring, dicentric or isochromosome Q93.2 Deletion of short arm of chromosome 4 Q93.3 Deletion of short arm of chromosome 5 Q93.4 Other deletions of part of a chromosome Q93.5 Angelman syndrome Q93.51 Phelan-McDermid syndrome Q93.52 Other deletions of part of a chromosome Q93.59 Deletions with other complex rearrangements Q93.7 Other deletions from the autosomes Q93.8 Velo-cardio-facial syndrome Q93.81 Williams syndrome Q93.82 Other microdeletions Q93.88 Other deletions from the autosomes Q93.89 Deletion from autosomes, unspecified Q93.9 Balanced rearrangements and structural markers, not elsewhere classified Q95 Balanced translocation and insertion in normal individual Q95.0 Chromosome inversion in normal individual Q95.1 Balanced autosomal rearrangement in abnormal individual Q95.2 Balanced sex/autosomal rearrangement in abnormal individual Q95.3 Individual with autosomal fragile site Q95.5 Other balanced rearrangements and structural markers Q95.8 Balanced rearrangement and structural marker, unspecified Q95.9 Turner's syndrome Q96 Karyotype 45, X Q96.0 Karyotype 46, X iso (Xq) Q96.1 Karyotype 46, X with abnormal sex chromosome, except iso (Xq) Q96.2 Mosaicism, 45, X/46, XX or XY Q96.3 Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome Q96.4 Other variants of Turner's syndrome Q96.8 Turner's syndrome, unspecified Q96.9 Other sex chromosome abnormalities, female phenotype, not elsewhere classified Q97 Karyotype 47, XXX Q97.0 Female with more than three X chromosomes Q97.1 Mosaicism, lines with various numbers of X chromosomes Q97.2 Female with 46, XY karyotype Q97.3 Other specified sex chromosome abnormalities, female phenotype Q97.8 Sex chromosome abnormality, female phenotype, unspecified Q97.9 Other sex chromosome abnormalities, male phenotype, not elsewhere classified Q98 Klinefelter syndrome karyotype 47, XXY Q98.0 Klinefelter syndrome, male with more than two X chromosomes Q98.1 Other male with 46, XX karyotype Q98.3 Klinefelter syndrome, unspecified Q98.4 Karyotype 47, XYY Q98.5 Male with structurally abnormal sex chromosome Q98.6 Male with sex chromosome mosaicism Q98.7 Other specified sex chromosome abnormalities, male phenotype Other specified sex chromosome abnormalities, male phenotype Q98.8 Sex chromosome abnormality, male phenotype, unspecified Q98.9 Other chromosome abnormalities, not elsewhere classified Q99