|OBO ID: DOID:0090086|
|Term Name:||hypogonadotropic hypogonadism 6 with or without anosmia||Search Ontology:|
|Definition:||A hypogonadotropic hypogonadism that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the FGF8 gene on chromosome 10q24, sometimes in association with mutation in another gene. https://www.ncbi.nlm.nih.gov/pubmed/18596921|
|Ontology:||Human Disease (DOID:0090086)|
|is a type of:||
OTHER hypogonadotropic hypogonadism 6 with or without anosmia PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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