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| Term | multiple endocrine neoplasia type 2B | ID (Ontology) | DOID:10016 (Human Disease) | |||||||||||||||||||||||||||
| Definition | A multiple endocrine neoplasia characterized by medullary thyroid carcinoma, pheochromocytoma, multiple mucosal neuromas and intestinal ganglioneuromas, and often a marfanoid habitus and other skeletal abnormalities. | |||||||||||||||||||||||||||||
| Also Known As | "MEN type IIB" ; "MEN2B" ; "mucosal neuroma 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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autosomal genetic disease |__autosomal dominant disease____ syndrome | |__multiple endocrine neoplasia__| multiple endocrine neoplasia type 2B 60 rec. |
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autosomal dominant disease multiple endocrine neoplasia |
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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ICD10CM:E31.23 ICD9CM:258.03 MESH:D018814 MIM:162300 NCI:C3227 ORDO:247709 SNOMEDCT_US_2023_03_01:61530001 UMLS_CUI:C0025269 |
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