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DO Term : familial medullary thyroid carcinoma [DOID:0050547] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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,
OMIM:155240,
MESH:C536911,
155240

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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