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Human Disease

hypogonadotropic hypogonadism 3 with or without anosmia

Term ID
DOID:0090092
Synonyms
Definition
A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the PROKR2 gene on chromosome 20p12, sometimes in association with mutation in another gene. (2)
References
Ontology
Human Disease   ( DOID:0090092 )
Relationships
is a type of
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Genes Involved
Zebrafish Models