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758.6 GONADAL DYSGENESIS


Code Information

Diagnosis Code: 758.6

Short Description: Gonadal dysgenesis

Long Description: Gonadal dysgenesis

Code Classification:

  • Congenital anomalies (740–759)
    • Congenital anomalies (740-759)
      • 758 Chromosomal anomalies
        • 758.6 Gonadal dysgenesis

Code Version: 2015 ICD-9-CM


References to Index of Diseases and Injuries

The code 758.6 has the following ICD-9-CM references to the Index of Diseases and Injuries
  • Absence (organ or part) (complete or partial)
    • gonadal, congenital NEC 758.6
  • Agenesis - see also Absence, by site, congenital
    • gonadal 758.6
  • Anomaly, anomalous (congenital) (unspecified type) 759.9
    • chromosomes, chromosomal 758.9
      • sex 758.81
        • complement, XO 758.6
        • gonadal dysgenesis 758.6
        • Turner's 758.6
  • Bonnevie-Ullrich syndrome 758.6
  • Deficiency, deficient
    • short stature homeobox gene (SHOX)
      • with
        • Turner's syndrome 758.6
  • Dwarf, dwarfism 259.4
    • ovarian 758.6
  • Dysgenesis
    • gonadal (due to chromosomal anomaly) 758.6
      • pure 752.7
    • ovarian 758.6
    • seminiferous tubules 758.6
  • OX syndrome 758.6
  • Syndrome - see also Disease
    • Bonnevie-Ullrich 758.6
    • OX 758.6
    • pterygolymphangiectasia 758.6
    • Turner's 758.6
    • Turner-Varny 758.6
    • Ullrich (-Bonnevie) (-Turner) 758.6
    • XO 758.6
  • Turner's
    • syndrome 758.6
  • Turner-Varny syndrome 758.6
  • Ullrich (-Bonnevie) (-Turner) syndrome 758.6
  • XO syndrome 758.6

Crosswalk Information

The code 758.6 converts into the following ICD-10 code(s):
ICD-9 Code ICD-10 Code ICD-10 Description
758.6 Right Arrow Q96.9 Turner's syndrome, unspecified
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
758.7 Klinefelter's syndrome
758.81 Other conditions due to sex chromosome anomalies
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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