Diagnoses (ICD-10-CM 2018)

Relevance Code Description
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
Q80.1 X-linked ichthyosis
E71.52 X-linked adrenoleukodystrophy
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
Q96.1 Karyotype 46, X iso (Xq)
E71.520 Childhood cerebral X-linked adrenoleukodystrophy
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