OBO ID: DOID:0090072
Term Name: hypogonadotropic hypogonadism 12 with or without anosmia Search Ontology:
Synonyms:
  • familial hypogonadotrophic eunuchoidism
  • familial idiopathic gonadotrpin deficiency
Definition: A hypogonadotropic hypogonadism that has_material_basis_in homozygous mutation in the GNRH1 gene on chromosome 8p21. https://www.ncbi.nlm.nih.gov/pubmed/19535795
References:
Ontology: Human Disease   (DOID:0090072)
OTHER hypogonadotropic hypogonadism 12 with or without anosmia PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GNRH1 ?Hypogonadotropic hypogonadism 12 with or without anosmia 614841
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None