Metadata | |
---|---|
ID | DOID:0112259 |
Name | Leydig cell hypoplasia |
Definition | A pseudohermaphroditism that has_material_basis_in homozygous or compound heterozygous mutation in the LHCGR gene on chromosome 2p16.3. https://medlineplus.gov/genetics/condition/leydig-cell-hypoplasia/, https://pubmed.ncbi.nlm.nih.gov/7719343/ |
Xrefs |
MEDDRA:10024406 |
Subsets |
DO_rare_slim |
Synonyms |
46,XY disorder of sex development due to LH resistance or LHB deficiency [EXACT] 46,XY disorder of sex development due to luteinizing hormone resistance or luteinizing hormone beta subunit deficiency [EXACT] 46,XY DSD due to LH resistance or LHB deficiency [EXACT] 46,XY DSD due to luteinizing hormone resistance or luteinizing hormone beta subunit deficiency [EXACT] |
Parent Relationships |