Search Ontology:
Human Disease

hypogonadotropic hypogonadism 12 with or without anosmia

Term ID
DOID:0090072
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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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