OBO ID: DOID:0090079
Term Name: hypogonadotropic hypogonadism 17 with or without anosmia Search Ontology:
Synonyms:
Definition: A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the SPRY4 gene on chromosome 5q31, sometimes in association with mutations in other genes. https://www.ncbi.nlm.nih.gov/pubmed/23643382
References:
Ontology: Human Disease   ( DOID:0090079 )
Relationships
is a type of:
OTHER hypogonadotropic hypogonadism 17 with or without anosmia PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SPRY4 Hypogonadotropic hypogonadism 17 with or without anosmia 615266
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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