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Human Disease

hypogonadotropic hypogonadism 20 with or without anosmia

Term ID
DOID:0090082
Synonyms
Definition
A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the FGF17 gene on chromosome 8p21, sometimes in association with mutations in other genes. https://www.ncbi.nlm.nih.gov/pubmed/23643382
References
Ontology
Human Disease   ( DOID:0090082 )
Relationships
is a type of
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Genes Involved
Zebrafish Models