|
Q99.2 |
Fragile X chromosome |
|
C96.6 |
Unifocal Langerhans-cell histiocytosis |
|
C96.0 |
Multifocal and multisystemic (disseminated) Langerhans-cell histiocytosis |
|
E88.81 |
Metabolic syndrome |
|
|
|
D82.3 |
Immunodeficiency following hereditary defective response to Epstein-Barr virus |
|
Q96.0 |
Karyotype 45, X |
|
E71.52 |
X-linked adrenoleukodystrophy |
|
Q80.1 |
X-linked ichthyosis |
|
C96.5 |
Multifocal and unisystemic Langerhans-cell histiocytosis |
|
W88.0 |
Exposure to X-rays |
|
Q96.2 |
Karyotype 46, X with abnormal sex chromosome, except iso (Xq) |
|
Z91.041 |
Radiographic dye allergy status |
|
|
|
E70.310 |
X-linked ocular albinism |
|
E71.521 |
Adolescent X-linked adrenoleukodystrophy |
|
E71.528 |
Other X-linked adrenoleukodystrophy |
|
E71.520 |
Childhood cerebral X-linked adrenoleukodystrophy |
|
Q96.1 |
Karyotype 46, X iso (Xq) |
|
E71.529 |
X-linked adrenoleukodystrophy, unspecified type |
|
Q96.3 |
Mosaicism, 45, X/46, XX or XY |
|
Q97.1 |
Female with more than three X chromosomes |
|
|
|
Q97.2 |
Mosaicism, lines with various numbers of X chromosomes |
|
D80.0 |
Hereditary hypogammaglobulinemia |
|
Q98.1 |
Klinefelter syndrome, male with more than two X chromosomes |
|
Q96.4 |
Mosaicism, 45, X/other cell line(s) with abnormal sex chromosome |
|
G11.1 |
Early-onset cerebellar ataxia |