ZFIN Human Disease: Leydig cell hypoplasia

OBO ID: DOID:0112259

Term Name:	Leydig cell hypoplasia		Search Ontology:
Synonyms:	46,XY disorder of sex development due to LH resistance or LHB deficiency 46,XY disorder of sex development due to luteinizing hormone resistance or luteinizing hormone beta subunit deficiency 46,XY DSD due to LH resistance or LHB deficiency 46,XY DSD due to luteinizing hormone resistance or luteinizing hormone beta subunit deficiency
Definition:	A pseudohermaphroditism that has_material_basis_in homozygous or compound heterozygous mutation in the LHCGR gene on chromosome 2p16.3. (2)
References:	GARD:3244 MEDDRA:10024406 MESH:C562567 ORDO:755
Ontology:	Human Disease ( DOID:0112259 )

Relationships

is a type of:	autosomal recessive disease pseudohermaphroditism autosomal recessive disease pseudohermaphroditism Show first 5 Terms
has subtype:	Leydig cell hypoplasia type I Leydig cell hypoplasia type II Leydig cell hypoplasia type I Leydig cell hypoplasia type II Show first 5 Terms

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Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None