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Disease Ontology Browser
multiple endocrine neoplasia type 2A (DOID:0050430)
Synonyms: MEN2A; multiple endocrine neoplasia II; Sipple syndrome
Alt IDs: OMIM:171400, ICD10CM:E31.22, ICD9CM:258.02, MESH:D018813, NCI:C3226, ORDO:247698, UMLS_CUI:C0025268
Definition: An autosomal dominant disease characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
07/11/2017
MGI 6.10
The Jackson Laboratory