Disease: Rhabdomyolysis ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Rhabdomyolysis
CUI: C0035410
Disease: Rhabdomyolysis
0.700 GeneticVariation CLINVAR Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases. 28779239 2017