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Intermediate nemaline myopathy
4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Congenital myopathy, Paradas type
1 associated gene
No signs/symptoms info
Intermediate nemaline myopathy
Congenital myopathy, Paradas type

ACTA1
(UniProt - OMIM)
 DYSF
(UniProt - OMIM)
KLHL41
(UniProt - OMIM)
NEB
(UniProt - OMIM)
TPM3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
NEB
(0.65)
DYSF


Citations in the biomedical literature:


Intermediate nemaline myopathy
ACTA1 KLHL41 NEB TPM3
Congenital myopathy, Paradas type
DYSF



Intermediate nemaline myopathy
Congenital myopathy, Paradas type

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: neonatal/infancy
Average age of death: any age
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.