reflex sympathetic dystrophy 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_1811)
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18 genes co-occuring with the disease reflex sympathetic dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
CALCA calcitonin-related polypeptide alpha 1.84954
GABBR1 gamma-aminobutyric acid (GABA) B receptor, 1 1.22909
NPS neuropeptide S 1.19748
ADAM2 ADAM metallopeptidase domain 2 0.988114
SYCP3 synaptonemal complex protein 3 0.97212
PRSS50 protease, serine, 50 0.9696
NPY neuropeptide Y 0.798282
TAC1 tachykinin, precursor 1 0.775341
RPIA ribose 5-phosphate isomerase A 0.632384
GPI glucose-6-phosphate isomerase 0.32993
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein 0.310652
GPC3 glypican 3 0.304864
BGLAP bone gamma-carboxyglutamate (gla) protein 0.269753
FLNA filamin A, alpha 0.230409
CD27 CD27 molecule 0.215653
CABIN1 calcineurin binding protein 1 0.173314
MPO myeloperoxidase 0.169091
PTH parathyroid hormone 0.160574