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| Term | Wolfram syndrome | ID (Ontology) | DOID:10632 (Human Disease) |
| Definition | A syndrome that is characterized by diabetes mellitus, optic atrophy, and deafness. | ||
| Also Known As | "WFS" | ||
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| DO.org | |||
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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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No relevant statements available
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disease |__syndrome |__Wolfram syndrome 11 rec. |__autosomal dominant Wolfram syndrome 1 rec. |__Wolfram syndrome 1 9 rec. |__Wolfram syndrome 2 2 rec. |__Wolfram syndrome, mitochondrial form |
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| Is a | syndrome | ||
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External Crossreferences & Linkouts
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GARD:7898 MESH:D014929 NCI:C35133 ORDO:3463 SNOMEDCT_US_2023_03_01:70694009 UMLS_CUI:C0043207 |
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