Chromosomal abnormalities, not elsewhere classified

Q90 Down's syndrome

• Q90 Down's syndrome
• Q90.0 Trisomy 21, meiotic nondisjunction
• Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)
• Q90.2 Trisomy 21, translocation
• Q90.9 Down's syndrome, unspecified

Q91 Edwards' syndrome and Patau's syndrome

• Q91 Edwards' syndrome and Patau's syndrome
• Q91.0 Trisomy 18, meiotic nondisjunction
• Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)
• Q91.2 Trisomy 18, translocation
• Q91.3 Edwards' syndrome, unspecified
• Q91.4 Trisomy 13, meiotic nondisjunction
• Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)
• Q91.6 Trisomy 13, translocation
• Q91.7 Patau's syndrome, unspecified

Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified

• Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified
• Q92.0 Whole chromosome trisomy, meiotic nondisjunction
• Q92.1 Whole chromosome trisomy, mosaicism (mitotic nondisjunction)
• Q92.2 Major partial trisomy
• Q92.3 Minor partial triosmy
• Q92.4 Duplications seen only at prometaphase
• Q92.5 Duplications with other complex rearrangements
• Q92.6 Extra marker chromosomes
• Q92.7 Triploidy and polyploidy
• Q92.8 Other specified trispmies and partial trisomies of autosomes
• Q92.9 Trisomy and partial trisomy of autosomes, unspecified

Q93 Monosomies and deletions from the autosomes, not elsewhere classified

• Q93 Monosomies and deletions from the autosomes, not elsewhere classified
• Q93.0 Whole chromosome monosomy, meiotic nondisjunction
• Q93.1 Whole chromosome monosomy, mosaicism (mitotic nondisjunction)
• Q93.2 Chromosome replaced with ring or dicentric
• Q93.3 Deletion of short arm of chromosome 4
• Q93.4 Deletion of short arm of chromosome 5
• Q93.5 Other deletions of part of a chromosome
• Q93.6 Deletions seen only at prometaphase
• Q93.7 Deletions with other complex rearrangements
• Q93.8 Other deletions from the autosomes
• Q93.9 Deletion from autosomes, unspecified

Q95 Balanced rearrangements and structural markers, not elsewhere classified

• Q95 Balanced rearrangements and structural markers, not elsewhere classified
• Q95.0 Balanced translocation and insertion in normal individual
• Q95.1 Chromosome inversion in normal indivedual
• Q95.2 Balanced autosomal rearrangement in abnormal individual
• Q95.3 Balanced sex/autosomal rearrangement in abnormal individual
• Q95.4 Individuals with marker heterochromatin
• Q95.5 Individuals with autosomal fragile site
• Q95.8 Other balanced rearrangements and stuctural markers
• Q95.9 Balanced rearrangement and structural marker, unspecified

Q96 Turner's syndrome

• Q96 Turner's syndrome
• Q96.0 Karyotype 45,X
• Q96.1 Karyotype 46,X iso (Xq)
• Q96.2 Karyotype 46,X with abnormal sex chromosome, except iso (Xq)
• Q96.3 Mosaicism, 45,X/46,XX or XY
• Q96.4 Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome
• Q96.8 Other variants of Turner's syndrome
• Q96.9 Turner's syndrome, unspecified

Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified

• Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified
• Q97.0 Karyotype 47,XXX
• Q97.1 Female with more than three X chromosomes
• Q97.2 Mosaicism, lines with various numbers of X chromosomes
• Q97.3 Female with 46,XY karyotype
• Q97.8 Other specified sex chromosome abnormalities, female phenotype
• Q97.9 Sex chromosome abnormality, female phenotype, unspecified

Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified

• Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified
• Q98.0 Klinefelter's syndrome karyotype 47,XXY
• Q98.1 Klinefelter,s syndrome, male with more than two X chromosomes
• Q98.2 Klinefelter's syndriome, male with 46,XX karyotype
• Q98.3 Other male with 46,XX karyotype
• Q98.4 Klinefelter's syndrome, unspecified
• Q98.5 Karyotype 47,XYY
• Q98.6 Male with structurally abnormal sex chromosome
• Q98.7 Male with sex chromosome mosaicism
• Q98.8 Other specified sex chromosome abnormalities, male phenotype
• Q98.9 Sex chromosome abnormality, male phenotype, unspecified

Q99 Other chromosome abnormalities,,not elsewhere classified

• Q99 Other chromosome abnormalities,,not elsewhere classified
• Q99.0 Chimera 46,XX/46,XY
• Q99.1 46,XX true hermaphrodite
• Q99.2 Fragile X chromosome
• Q99.8 Other specified chromosome abnormalities
• Q99.9 Chromosomal abnormality,unspecified