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Echinobase
Summary Literature (0)
DOID:0050430 - multiple endocrine neoplasia type 2A

Disease Ontology Definition:An autosomal dominant disease characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis.

Synonyms: MEN2A, Sipple syndrome, multiple endocrine neoplasia II,

Echinobase Genes : ret


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

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a)