OBO ID: DOID:0090085 |
Term Name: | hypogonadotropic hypogonadism 9 with or without anosmia | Search Ontology: | |
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Definition: | A hypogonadotropic hypogonadism that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the NELF gene on chromosome 9q34, sometimes in association with mutation in another gene. (2) | ||
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Ontology: | Human Disease ( DOID:0090085 ) |
OTHER hypogonadotropic hypogonadism 9 with or without anosmia PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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