OBO ID: DOID:0090086
Term Name: hypogonadotropic hypogonadism 6 with or without anosmia Search Ontology:
Synonyms:
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
References:
Ontology: Human Disease   ( DOID:0090086 )
Relationships
is a type of:
OTHER hypogonadotropic hypogonadism 6 with or without anosmia PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FGF8 Hypogonadotropic hypogonadism 6 with or without anosmia 612702
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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