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Leydig cell hypoplasia due to complete LH resistance

ORPHA:96265

Classification level: Subtype of disorder
  • Synonym(s):
    • 46,XY DSD due to complete LH receptor inactivation
    • 46,XY DSD due to complete LH resistance
    • 46,XY DSD due to complete luteinizing hormone receptor inactivation
    • 46,XY DSD due to complete luteinizing hormone resistance
    • 46,XY disorder of sex development due to complete LH receptor inactivation
    • 46,XY disorder of sex development due to complete LH resistance
    • 46,XY disorder of sex development due to complete luteinizing hormone receptor inactivation
    • 46,XY disorder of sex development due to complete luteinizing hormone resistance
    • Leydig cell hypoplasia due to complete LH receptor inactivation
    • Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation
    • Leydig cell hypoplasia due to complete luteinizing hormone resistance
  • Prevalence: -
  • Inheritance: -
  • Age of onset: Neonatal
  • ICD-10: Q56.1
  • OMIM: 238320
  • UMLS: -
  • MeSH: -
  • GARD: -
  • MedDRA: -

Summary

An Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional Information menu located at the bottom of this page.

Additional information

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The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.