Dataset | CTD Gene-Disease Associations |
Category | disease or phenotype associations |
Type | disease |
Description | An autosomal dominant disease characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis. (Human Disease Ontology, DOID_0050430) |
External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D018813 |
Similar Terms | |
Downloads & Tools |
1 genes/proteins associated with the disease Multiple Endocrine Neoplasia Type 2a from the curated CTD Gene-Disease Associations dataset.
Symbol | Name | Standardized Value |
---|---|---|
RET | ret proto-oncogene | 2.88009 |