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| Term | Kallmann syndrome | ID (Ontology) | DOID:3614 (Human Disease) |
| Definition | A hypogonadotropic hypogonadism with a defective sense of smell (anosmia or hyposmia). | ||
| Also Known As | "familial hypogonadism with anosmia" ; "Hypogonadism with anosmia" ; "Kallman syndrome" (for all, see Synonyms field below) | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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hypogonadism |__hypogonadotropic hypogonadism |__Kallmann syndrome |
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| Is a | hypogonadotropic hypogonadism | ||
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External Crossreferences & Linkouts
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GARD:10771 ICD10CM:E23.0 MESH:D017436 NCI:C75479 ORDO:478 SNOMEDCT_US_2023_03_01:190559001 UMLS_CUI:C0162809 |
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