Condition: Rhabdomyolysis
rs121918608
in
AHCY
gene and
Rhabdomyolysis
PMID 28779239
2017 Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases.
rs867410737
in
ATP5F1D
gene and
Rhabdomyolysis
PMID 29478781
2018 Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.
rs763794604
in
CACNA1S
gene and
Rhabdomyolysis
PMID 28779239
2017 Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases.
rs74315294
in
CPT2
gene and
Rhabdomyolysis
PMID 28779239
2017 Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases.
rs750422335
in
DBNL;PGAM2
gene and
Rhabdomyolysis
PMID 28779239
2017 Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases.
rs202143236
in
PFKM;MIR6505
gene and
Rhabdomyolysis
PMID 28779239
2017 Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases.
rs1555762532
in
RYR1
gene and
Rhabdomyolysis
PMID 28779239
2017 Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases.
rs2819742
in
RYR2
gene and
Rhabdomyolysis
PMID 21386754
2011 Cerivastatin, genetic variants, and the risk of rhabdomyolysis.
rs121908545
in
SCN4A
gene and
Rhabdomyolysis
PMID 28779239
2017 Exome sequencing in Jewish and Arab patients with rhabdomyolysis reveals single-gene etiology in 43% of cases.
rs752298579
in
TANGO2
gene and
Rhabdomyolysis
PMID 26805781
2016 Recurrent Muscle Weakness with Rhabdomyolysis, Metabolic Crises, and Cardiac Arrhythmia Due to Bi-allelic TANGO2 Mutations.