Orphanet: Leydig cell hypoplasia due to complete LH resistance

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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

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Leydig cell hypoplasia due to complete LH resistance

ORPHA:96265

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