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Human Disease

hypogonadotropic hypogonadism 22 with or without anosmia

Term ID
DOID:0090081
Synonyms
Definition
A hypogonadotropic hypogonadism that has_material_basis_in homozygous mutation in the FEZF1 gene on chromosome 7q31. https://www.ncbi.nlm.nih.gov/pubmed/25192046
References
Ontology
Human Disease   ( DOID:0090081 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models