facial hemiatrophy Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_1757)
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Genes

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

Symbol Name Standardized Value
COPS2 COP9 signalosome subunit 2 1.44123
CTSC cathepsin C 1.22345
HARS histidyl-tRNA synthetase 1.22085
ARHGEF1 Rho guanine nucleotide exchange factor (GEF) 1 1.00541
SNRNP70 small nuclear ribonucleoprotein 70kDa (U1) 0.95996
COL17A1 collagen, type XVII, alpha 1 0.76431
HMGA2 high mobility group AT-hook 2 0.751271
PIGA phosphatidylinositol glycan anchor biosynthesis, class A 0.643797