Brachyolmia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An osteochondrodysplasia characterized by generalized platyspondyly without significant long bone abnormalities and short stature. (Human Disease Ontology, DOID_0050690)
External Link https://www.disgenet.org/browser/0/1/0/C0432228
Similar Terms
Downloads & Tools

Genes

3 genes associated with the disease Brachyolmia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
LTBP3 latent transforming growth factor beta binding protein 3
PAPSS2 3'-phosphoadenosine 5'-phosphosulfate synthase 2
TRPV4 transient receptor potential cation channel, subfamily V, member 4