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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

Xenbase Genes : ret, esr2, ntrk1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007958 - familial medullary thyroid carcinoma

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)