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Echinobase
Summary Literature (0)
DOID:0050547 - familial medullary thyroid carcinoma

Disease Ontology Definition:A thyroid gland medullary carcinoma that has_material_basis_in a mutation in the RET gene on chromosome 10. Familial MTC can also be caused by mutations in the NTRK1 gene located on 1q21-q22.

Synonyms: THYROID CARCINOMA, FAMILIAL MEDULLARY

Echinobase Genes : ret


MIM:
MIM:155240 - thyroid carcinoma, familial medullary; mtc

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), medullary thyroid carcinoma (is_a)