Search Ontology: 
        
        Human Disease
            hypogonadotropic hypogonadism 2 with or without anosmia
- Term ID
- DOID:0090083
- Synonyms
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- 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
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    - ICD10CM:E23.0
- MIM:147950
 
- Ontology
- Human Disease ( DOID:0090083 )
                
                    
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