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| Term | tuberous sclerosis | ID (Ontology) | DOID:13515 (Human Disease) |
| Definition | A hamartoma syndrome that is characterized by the growth of numerous noncancerous tumors in many parts of the body. | ||
| Also Known As | "Bourneville's disease" ; "cerebral sclerosis" ; "Epiloia" (for all, see Synonyms field below) | ||
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| Annotations | |||
| 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__ syndrome | |__hamartoma syndrome__________| tuberous sclerosis 33 rec. |__tuberous sclerosis 1 4 rec. |__tuberous sclerosis 2 3 rec. |
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Relationships
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| Is a |
autosomal dominant disease hamartoma syndrome |
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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GARD:7830 ICD10CM:Q85.1 ICD9CM:759.5 MESH:D014402 MIM:PS191100 NCI:C3424 SNOMEDCT_US_2023_03_01:157033002 UMLS_CUI:C0041341 |
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