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Brody myopathy
Brody myopathy
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
BRODY DISEASE
601003
ATP2A1
Unknown
—
HPO
Calcium signaling pathway
cGMP-PKG signaling pathway
cAMP signaling pathway
Efferocytosis
Cardiac muscle contraction
Adrenergic signaling in cardiomyocytes
Osteoclast differentiation
Thyroid hormone signaling pathway
Pancreatic secretion
Alzheimer disease
Spinocerebellar ataxia
Pathways of neurodegeneration - multiple diseases
Hypertrophic cardiomyopathy
Arrhythmogenic right ventricular cardiomyopathy
Dilated cardiomyopathy
Diabetic cardiomyopathy
Reduction of cytosolic Ca++ levels
Ion homeostasis
Ion transport by P-type ATPases
+16 more
BRODY MYOPATHY
C1832918
RABEP2
Unknown
—
Disgenet
—
All
2
Causal
1
Unknown
2
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
1
CTD
0
HPO
1
GWAS catalog
0
GenCC
0
ClinGen
0
Related Diseases
Diseases that share the most curated genes with Brody myopathy.
5
View disease cluster →
Hypogonadism
1 shared gene
ATP2A1
Related via 1 shared gene including ATP2A1.
Glomerulonephritis
1 shared gene
RABEP2
Related via 1 shared gene including RABEP2.
Congestive heart failure
1 shared gene
ATP2A1
Related via 1 shared gene including ATP2A1.
Heart failure
1 shared gene
ATP2A1
Related via 1 shared gene including ATP2A1.
Parkinson disease
1 shared gene
RABEP2
Related via 1 shared gene including RABEP2.
1
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