|
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
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)