Native American Myopathy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Native American myopathy (NAM) is a neuromuscular disorder characterized by weakness, arthrogryposis, kyphoscoliosis, short stature, cleft palate, ptosis and susceptibility to malignant hyperthermia during anesthesia. (Orphanet Rare Disease Ontology, Orphanet_168572)
External Link https://www.disgenet.org/browser/0/1/0/C1850625
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Genes

6 genes associated with the disease Native American Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
G6PD glucose-6-phosphate dehydrogenase
NINJ1 ninjurin 1
PPARGC1A peroxisome proliferator-activated receptor gamma, coactivator 1 alpha
RYR1 ryanodine receptor 1 (skeletal)
SIRT1 sirtuin 1
STAC3 SH3 and cysteine rich domain 3