ZFIN Human Disease: hypogonadotropic hypogonadism 24 without anosmia

OBO ID: DOID:0090088

Term Name:	hypogonadotropic hypogonadism 24 without anosmia		Search Ontology:
Synonyms:	isolated follicle-stimulating hormone deficiency
Definition:	A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the FSHB gene on chromosome 11p14. (2)
References:	ICD10CM:E23.6 OMIM:229070 ORDO:52901
Ontology:	Human Disease ( DOID:0090088 )

Relationships

is a type of:	autosomal recessive disease hypogonadotropic hypogonadism autosomal recessive disease hypogonadotropic hypogonadism Show first 5 Terms

OTHER hypogonadotropic hypogonadism 24 without anosmia PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
FSHB	fshb	Hypogonadotropic hypogonadism 24 without anosmia	229070

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None