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Q84.2 Other congenital malformations of hair |
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Q84.3 Anonychia |
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Q84.4 Congenital leukonychia |
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Q84.5 Enlarged and hypertrophic nails |
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Q84.6 Other congenital malformations of nails |
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Q84.8 Other specified congenital malformations of integument |
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Q84.9 Congenital malformation of integument, unspecified |
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Q85.00 Neurofibromatosis, unspecified |
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Q85.01 Neurofibromatosis, type 1 |
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Q85.02 Neurofibromatosis, type 2 |
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Q85.03 Schwannomatosis |
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Q85.09 Other neurofibromatosis |
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Q85.1 Tuberous sclerosis |
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Q85.8 Other phakomatoses, not elsewhere classified |
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Q85.9 Phakomatosis, unspecified |
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Q86.0 Fetal alcohol syndrome (dysmorphic) |
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Q86.1 Fetal hydantoin syndrome |
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Q86.2 Dysmorphism due to warfarin |
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Q86.8 Other congenital malformation syndromes due to known exogenous causes |
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Q87.0 Congenital malformation syndromes predominantly affecting facial appearance |
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Q87.11 Prader-Willi syndrome |
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Q87.19 Other congenital malformation syndromes predominantly associated with short stature |
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Q87.2 Congenital malformation syndromes predominantly involving limbs |
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Q87.3 Congenital malformation syndromes involving early overgrowth |
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Q87.40 Marfan's syndrome, unspecified |
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Q87.410 Marfan's syndrome with aortic dilation |
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Q87.418 Marfan's syndrome with other cardiovascular manifestations |
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Q87.42 Marfan's syndrome with ocular manifestations |
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Q87.43 Marfan's syndrome with skeletal manifestation |
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Q87.5 Other congenital malformation syndromes with other skeletal changes |
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Q87.81 Alport syndrome |
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Q87.82 Arterial tortuosity syndrome |
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Q87.89 Other specified congenital malformation syndromes, not elsewhere classified |
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Q89.01 Asplenia (congenital) |
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Q89.09 Congenital malformations of spleen |
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Q89.1 Congenital malformations of adrenal gland |
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Q89.2 Congenital malformations of other endocrine glands |
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Q89.3 Situs inversus |
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Q89.4 Conjoined twins |
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Q89.7 Multiple congenital malformations, not elsewhere classified |
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Q89.8 Other specified congenital malformations |
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Q89.9 Congenital malformation, unspecified |
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Q90.0 Trisomy 21, nonmosaicism (meiotic nondisjunction) |
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Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction) |
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Q90.2 Trisomy 21, translocation |
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Q90.9 Down syndrome, unspecified |
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Q91.0 Trisomy 18, nonmosaicism (meiotic nondisjunction) |
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Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction) |
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Q91.2 Trisomy 18, translocation |
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Q91.3 Trisomy 18, unspecified |
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Q91.4 Trisomy 13, nonmosaicism (meiotic nondisjunction) |
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Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction) |
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Q91.6 Trisomy 13, translocation |
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Q91.7 Trisomy 13, unspecified |
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Q92.0 Whole chromosome trisomy, nonmosaicism (meiotic nondisjunction) |
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Q92.1 Whole chromosome trisomy, mosaicism (mitotic nondisjunction) |
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Q92.2 Partial trisomy |
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Q92.5 Duplications with other complex rearrangements |
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Q92.61 Marker chromosomes in normal individual |
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Q92.62 Marker chromosomes in abnormal individual |
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Q92.7 Triploidy and polyploidy |
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Q92.8 Other specified trisomies and partial trisomies of autosomes |
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Q92.9 Trisomy and partial trisomy of autosomes, unspecified |
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Q93.0 Whole chromosome monosomy, nonmosaicism (meiotic nondisjunction) |
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Q93.1 Whole chromosome monosomy, mosaicism (mitotic nondisjunction) |
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Q93.2 Chromosome replaced with ring, dicentric or isochromosome |
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Q93.3 Deletion of short arm of chromosome 4 |
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Q93.4 Deletion of short arm of chromosome 5 |
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Q93.51 Angelman syndrome |
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Q93.59 Other deletions of part of a chromosome |
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Q93.7 Deletions with other complex rearrangements |
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Q93.81 Velo-cardio-facial syndrome |
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Q93.82 Williams syndrome |
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Q93.88 Other microdeletions |
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Q93.89 Other deletions from the autosomes |
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Q93.9 Deletion from autosomes, unspecified |
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Q95.0 Balanced translocation and insertion in normal individual |
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Q95.1 Chromosome inversion in normal individual |
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Q95.2 Balanced autosomal rearrangement in abnormal individual |
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Q95.3 Balanced sex/autosomal rearrangement in abnormal individual |
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Q95.5 Individual with autosomal fragile site |
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Q95.8 Other balanced rearrangements and structural markers |
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Q95.9 Balanced rearrangement and structural marker, unspecified |
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Q96.0 Karyotype 45, X |
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Q96.1 Karyotype 46, X iso (Xq) |
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Q96.2 Karyotype 46, X with abnormal sex chromosome, except iso (Xq) |
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Q96.3 Mosaicism, 45, X/46, XX or XY |
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Q96.4 Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome |
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Q96.8 Other variants of Turner's syndrome |
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Q96.9 Turner's syndrome, unspecified |
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Q97.0 Karyotype 47, XXX |
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Q97.1 Female with more than three X chromosomes |
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Q97.2 Mosaicism, lines with various numbers of X chromosomes |
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Q97.3 Female with 46, XY karyotype |
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Q97.8 Other specified sex chromosome abnormalities, female phenotype |
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Q97.9 Sex chromosome abnormality, female phenotype, unspecified |
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Q98.0 Klinefelter syndrome karyotype 47, XXY |
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Q98.1 Klinefelter syndrome, male with more than two X chromosomes |
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Q98.3 Other male with 46, XX karyotype |
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Q98.4 Klinefelter syndrome, unspecified |
