brachyolmia Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
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)
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Genes

7 genes co-occuring with the disease brachyolmia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
TRPV4 transient receptor potential cation channel, subfamily V, member 4 2.76535
PAPSS2 3'-phosphoadenosine 5'-phosphosulfate synthase 2 1.8459
WDR72 WD repeat domain 72 1.5194
GALNS galactosamine (N-acetyl)-6-sulfatase 0.86714
FST follistatin 0.73746
GLB1 galactosidase, beta 1 0.32701
MGAM maltase-glucoamylase 0.28151