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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

GARD:3244

MEDDRA:10024406

MESH:C562567

ORDO:755

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

is_a pseudohermaphroditism

is_a autosomal recessive disease

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