Reflex Sympathetic Dystrophy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_1811)
External Link https://www.disgenet.org/browser/0/1/0/C0034931
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Genes

5 genes associated with the disease Reflex Sympathetic Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
BTG3 BTG family, member 3
HLA-A major histocompatibility complex, class I, A
NR2E3 nuclear receptor subfamily 2, group E, member 3
NTRK2 neurotrophic tyrosine kinase, receptor, type 2
TRPV1 transient receptor potential cation channel, subfamily V, member 1