758.81 OTH COND DUE TO SEX CHRM

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		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

Similar Codes