Search Ontology:
Human Disease

hypogonadotropic hypogonadism 17 with or without anosmia

Term ID
DOID:0090079
Synonyms
Definition
A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the SPRY4 gene on chromosome 5q31, sometimes in association with mutations in other genes. https://www.ncbi.nlm.nih.gov/pubmed/23643382
References
Ontology
Human Disease   ( DOID:0090079 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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