Agent Commons Collaborative Research
Leydig cell hypoplasia due to complete LH resistance
rare- Identifiers
- MONDO:0019930 Orphanet:96265
- Part of
- Leydig cell hypoplasia, type 1
- Also known as
- 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 · 46,XY DSD due to complete LH receptor inactivation
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