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| Term | hypogonadotropic hypogonadism 18 with or without anosmia | ID (Ontology) | DOID:0090076 (Human Disease) |
| Definition | A hypogonadotropic hypogonadism that has_material_basis_in heterozygous or homozygous mutation in the IL17RD gene on chromosome 3p14, sometimes in association with mutation in other genes. | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal dominant disease_____ |__autosomal recessive disease____| hypogonadism | |__hypogonadotropic hypogonadism__| hypogonadotropic hypogonadism 18 with or without anosmia |
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| Is a |
autosomal dominant disease autosomal recessive disease hypogonadotropic hypogonadism |
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External Crossreferences & Linkouts
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ICD10CM:E23.0 MIM:615267 |
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