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| Term | multiple endocrine neoplasia type 2A | ID (Ontology) | DOID:0050430 (Human Disease) | |||||||||||||||||||||||||||
| Definition | A multiple endocrine neoplasia characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis. | |||||||||||||||||||||||||||||
| Also Known As | "MEN2A" ; "multiple endocrine neoplasia II" ; "Sipple syndrome" | |||||||||||||||||||||||||||||
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autosomal genetic disease |__autosomal dominant disease____ syndrome | |__multiple endocrine neoplasia__| multiple endocrine neoplasia type 2A 36 rec. |
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autosomal dominant disease multiple endocrine neoplasia |
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ICD10CM:E31.22 ICD9CM:258.02 MESH:D018813 MIM:171400 NCI:C3226 ORDO:247698 SNOMEDCT_US_2023_03_01:721188000 UMLS_CUI:C0025268 |
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