Parastremmatic dwarfism Gene Set

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
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Genes

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