multiple endocrine neoplasia type 2A

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Summary

Literature (0)

DOID:0050430 - multiple endocrine neoplasia type 2A

Disease Ontology Definition:A multiple endocrine neoplasia characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis.

Synonyms: MEN2A, multiple endocrine neoplasia II, Sipple syndrome

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: ret

MIM:

MIM:171400 - multiple endocrine neoplasia, type iia; men2a

MIM:171400 - multiple endocrine neoplasia, type iia; men2a

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), multiple endocrine neoplasia (is_a)