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758.81 OTH COND DUE TO SEX CHRM


Code Information

Diagnosis Code: 758.81

Short Description: Oth cond due to sex chrm

Long Description: Other conditions due to sex chromosome anomalies

Code Classification:

  • Congenital anomalies (740–759)
    • Congenital anomalies (740-759)
      • 758 Chromosomal anomalies
        • 758.81 Oth cond due to sex chrm

Code Version: 2015 ICD-9-CM


Synonyms

  • 18p partial monosomy syndrome
  • 46, XX true hermaphrodite
  • Absence of sex chromosome
  • Additional sex chromosome
  • Anomaly of chromosome X
  • Anomaly of chromosome Y
  • Anomaly of sex chromosome
  • Barr body absent, nuclear sex male
  • Barr body, more than one present per cell
  • Chimera 46, XX; 46, XY
  • Double Y syndrome
  • Female with more than three X chromosomes
  • Four X syndrome
  • Fragile X chromosome
  • FRAXA
  • FRAXE
  • Karyotype 46, X iso
  • Karyotype 46, X with abnormal sex chromosome except iso
  • Male with structurally abnormal sex chromosome
  • Mosaic including XXXXY
  • Mosaic XO/XX
  • Mosaic XO/XY
  • Mosaic XY/XXY
  • Mosaicism - lines with various numbers of X chromosomes
  • Mosaicism 45, X / other cell line with abnormal sex chromosome
  • Penta X syndrome
  • Sex chromosome abnormality - female phenotype
  • Sex chromosome abnormality - male phenotype
  • Sex chromosome mosaicism
  • Sex phenotype-karyotype dissociation syndrome
  • Sex-linked hereditary disorder
  • Tetrasomy 12p
  • Triple X syndrome, epilepsy, and hypogammaglobulinemia
  • Trisomy X syndrome
  • Virilization of female due to SOX9 gene duplication
  • Virilization of female due to SRY gene translocation
  • X-linked creatine deficiency
  • X-linked intellectual deficit-dystonia-dysarthria syndrome
  • XX males
  • XXXXY syndrome
  • XXXY syndrome
  • XXYY syndrome
  • XY females
  • XY, female phenotype

References to Index of Diseases and Injuries

The code 758.81 has the following ICD-9-CM references to the Index of Diseases and Injuries
  • Abnormal, abnormality, abnormalities - see also Anomaly
    • chromosomal NEC 758.89
      • sex 758.81
  • Absence (organ or part) (complete or partial)
    • breast(s) (acquired) V45.71
    • sex chromosomes 758.81
  • Accessory (congenital)
    • chromosome(s) NEC 758.5
      • sex 758.81
  • Additional - see also Accessory
    • chromosome(s) 758.5
      • sex 758.81
  • Anomaly, anomalous (congenital) (unspecified type) 759.9
    • chromosomes, chromosomal 758.9
      • sex 758.81
        • complement, XO 758.6
        • complement, XXX 758.81
        • complement, XXY 758.7
        • complement, XYY 758.81
        • gonadal dysgenesis 758.6
        • Klinefelter's 758.7
        • Turner's 758.6
    • sex chromosomes NEC (see also Anomaly, chromosomes) 758.81
  • Mosaicism, mosaic (chromosomal) 758.9
    • sex 758.81
  • Paratyphoid (fever) - see Fever, paratyphoid
  • Penta X syndrome 758.81
  • Sex chromosome mosaics 758.81
  • Syndrome - see also Disease
    • due to abnormality
      • chromosomal 758.89
        • sex 758.81
    • Penta X 758.81
    • sex chromosome mosaic 758.81
    • triplex X female 758.81
    • XXX 758.81
    • XXXXY 758.81
  • Triple - see also Accessory
    • X female 758.81
  • XXX syndrome 758.81
  • XXXXY syndrome 758.81
  • XYY syndrome 758.81

Crosswalk Information

The code 758.81 converts into the following ICD-10 code(s):
ICD-9 Code ICD-10 Code ICD-10 Description
758.81 Right Arrow Q97.0 Karyotype 47, XXX
Q97.1 Female with more than three X chromosomes
Q97.2 Mosaicism, lines with various numbers of X chromosomes
Q97.8 Oth sex chromosome abnormalities, female phenotype
Q98.5 Karyotype 47, XYY
Q98.7 Male with sex chromosome mosaicism
Q98.8 Other specified sex chromosome abnormalities, male phenotype
Q99.8 Other specified chromosome abnormalities
This ICD-9 to ICD-10 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-9 Code ICD-9 Description
758.0 Down's syndrome
758.1 Patau's syndrome
758.2 Edwards' syndrome
758.31 Cri-du-chat syndrome
758.32 Velo-cardio-facial syndrome
758.33 Other microdeletions
758.39 Other autosomal deletions
758.4 Balanced autosomal translocation in normal individual
758.5 Other conditions due to autosomal anomalies
758.6 Gonadal dysgenesis
758.7 Klinefelter's syndrome
758.89 Other conditions due to chromosome anomalies
758.9 Conditions due to anomaly of unspecified chromosome

This page was last updated on: 10/1/2014

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