Cytoscape Web
Click node...

Autosomal dominant limb-girdle muscular dystrophy type 1E
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Childhood-onset nemaline myopathy
6 associated genes
No signs/symptoms info
Autosomal dominant limb-girdle muscular dystrophy type 1E
Childhood-onset nemaline myopathy

DES
(UniProt - OMIM)
 ACTA1
(UniProt - OMIM)
KBTBD13
(UniProt - OMIM)
KLHL41
(UniProt - OMIM)
NEB
(UniProt - OMIM)
TPM2
(UniProt - OMIM)
TPM3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
DES
(0.75)
NEB


Citations in the biomedical literature:


Autosomal dominant limb-girdle muscular dystrophy type 1E
DES
Childhood-onset nemaline myopathy
ACTA1 KBTBD13 KLHL41 NEB TPM2 TPM3



Autosomal dominant limb-girdle muscular dystrophy type 1E
Childhood-onset nemaline myopathy

Synonym(s):
- LGMD1E
Synonym(s):
- Mild nemaline myopathy
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: no data available
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.