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Human Disease

hypogonadotropic hypogonadism 2 with or without anosmia

Term ID
DOID:0090083
Synonyms
Definition
A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the FGFR1 gene on chromosome 8p11, sometimes in association with mutation in other genes. (2)
References
Ontology
Human Disease   ( DOID:0090083 )
Relationships
is a type of
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Genes Involved
Zebrafish Models