| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Nephrogenic systemic fibrosis (NSF) is a rare systemic fibrosing condition observed in renally impaired patients and characterized by a hardening and thickening of the skin with fibrotic plaques or papules, pruritus, joint pain and stiffness, muscle weakness, limitation of range of motion, and yellowed eyes. It is generally associated with administration of gadolinium-based magnetic resonance imaging contrast agents (GBCA) in patients with kidney disease. (Orphanet Rare Disease Ontology, Orphanet_137617) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:D054989 |
| Similar Terms | |
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3 genes/proteins associated with the disease Nephrogenic Fibrosing Dermopathy from the curated CTD Gene-Disease Associations dataset.
