GeDiPNet
☰
Home
Browse
Genes
Diseases
Proteins
SNPs / Variants
Pathways ►
Reactome
KEGG
Analysis
Statistics
Resources
Blogs
Login
Contact Us
Search
Home
/
Diseases
/
Multiminicore myopathy
Multiminicore myopathy
Log in to bookmark this disease
Bookmark This Disease
Title
Project / Tag (optional)
Note (optional)
Cancel
Save
Download ▾
Download as CSV
Download as PDF
Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
CLASSIC MULTIMINICORE MYOPATHY
324604
C5679883
MYH7
Unknown
22784669
Disgenet
,
Orphanet
cGMP-PKG signaling pathway
Cardiac muscle contraction
Adrenergic signaling in cardiomyocytes
Motor proteins
Cytoskeleton in muscle cells
Thyroid hormone signaling pathway
Hypertrophic cardiomyopathy
Dilated cardiomyopathy
Viral myocarditis
+6 more
SELENON
Unknown
12192640
Disgenet
,
Orphanet
—
TTN
Unknown
24105469
Disgenet
,
Orphanet
Cytoskeleton in muscle cells
Hypertrophic cardiomyopathy
Dilated cardiomyopathy
Platelet degranulation
Striated Muscle Contraction
+2 more
All
3
Causal
0
Unknown
3
Select all
Clear
ClinVar
0
Orphanet
3
Disgenet
3
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
0
Related Diseases
Diseases that share the most curated genes with Multiminicore myopathy.
5
View disease cluster →
Myosin storage myopathy
1 shared gene
MYH7
Related via 1 shared gene including MYH7.
Biventricular noncompaction cardiomyopathy
1 shared gene
MYH7
Related via 1 shared gene including MYH7.
MYH7-related skeletal myopathy
1 shared gene
MYH7
Related via 1 shared gene including MYH7.
dilated cardiomyopathy 1S
1 shared gene
MYH7
Related via 1 shared gene including MYH7.
Progressive contractures limb-girdle weakness muscle dystrophy syndrome
1 shared gene
TTN
Related via 1 shared gene including TTN.
1
GeDiPNet AI Assistant
Online