Multiple endocrine neoplasia, type 2b Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An autosomal dominant disease characterized by medullary thyroid carcinoma, pheochromocytoma, multiple mucosal neuromas and intestinal ganglioneuromas, and often a marfanoid habitus and other skeletal abnormalities. (Human Disease Ontology, DOID_10016)
External Link http://www.omim.org/entry/162300
Similar Terms
Downloads & Tools

Genes

1 genes associated with the Multiple endocrine neoplasia, type 2b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
RET ret proto-oncogene