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| Term | branchiootorenal syndrome | ID (Ontology) | DOID:14702 (Human Disease) |
| Definition | A syndrome characterized by branchial arch anomalies (branchial fistulas, clefts, or cysts), hearing impairment, structural defects of the outer, middle, and inner ear, and renal abnormalities. | ||
| Also Known As | "Branchio-Oto-renal syndrome" ; "Branchio-otorenal dysplasia" ; "branchiootorenal dysplasia" (for all, see Synonyms field below) | ||
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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__ disease | |__syndrome____________________| branchiootorenal syndrome 7 rec. |__branchiootorenal syndrome 1 2 rec. |__branchiootorenal syndrome 2 1 rec. |
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| Is a |
autosomal dominant disease syndrome |
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External Crossreferences & Linkouts
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GARD:10147 MEDDRA:10071135 MESH:D019280 NCI:C98983 SNOMEDCT_US_2023_03_01:290006 UMLS_CUI:C0265234 |
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