ZFIN Human Disease: hypogonadotropic hypogonadism 18 with or without anosmia

OBO ID: DOID:0090076

Term Name:	hypogonadotropic hypogonadism 18 with or without anosmia		Search Ontology:
Synonyms:
Definition:	A hypogonadotropic hypogonadism that has_material_basis_in heterozygous or homozygous mutation in the IL17RD gene on chromosome 3p14, sometimes in association with mutation in other genes. https://www.ncbi.nlm.nih.gov/pubmed/23643382
References:	ICD10CM:E23.0 OMIM:615267
Ontology:	Human Disease ( DOID:0090076 )

Relationships

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

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Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
IL17RD	il17rd	Hypogonadotropic hypogonadism 18 with or without anosmia	615267

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None