Preferred Name | multiple endocrine neoplasia type 2A | |
Synonyms |
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Definitions |
An autosomal dominant disease characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis. OMIM mapping confirmed by DO. [SN]. |
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ID |
http://purl.obolibrary.org/obo/DOID_0050430 |
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comment |
OMIM mapping confirmed by DO. [SN]. |
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definition |
An autosomal dominant disease characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis. |
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hasDbXref |
UMLS_CUI:C0025268 ICD9CM:258.02 SNOMEDCT_US_2016_03_01:61808009 ORDO:247698 NCI:C3226 ICD10CM:E31.22 MESH:D018813 OMIM:171400 |
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hasExactSynonym |
multiple endocrine neoplasia II MEN2A Sipple syndrome |
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hasOBONamespace |
disease_ontology |
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id |
DOID:0050430 |
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imported from | ||
inSubset | ||
label |
multiple endocrine neoplasia type 2A |
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prefixIRI |
DOID:0050430 |
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prefLabel |
multiple endocrine neoplasia type 2A |
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subClassOf |
Create mapping