| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Parastremmatic dwarfism is a very rare chondrodysplasia characterized by severe dwarfism, kyphoscoliosis, stiffness of large joints and distortion of lower limbs. (Orphanet Rare Disease Ontology, Orphanet_2646) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C537172 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Parastremmatic dwarfism from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| TRPV4 | transient receptor potential cation channel, subfamily V, member 4 | 2.88009 |
