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Typical nemaline myopathy
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers
1 associated gene
No signs/symptoms info
Typical nemaline myopathy
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers

ACTA1
(UniProt - OMIM)
 DMD
(UniProt - OMIM)
CFL2
(UniProt - OMIM)
KLHL41
(UniProt - OMIM)
NEB
(UniProt - OMIM)
TPM2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ACTA1
(0.87)
DMD


Citations in the biomedical literature:


Typical nemaline myopathy
ACTA1 CFL2 KLHL41 NEB TPM2
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers
DMD



Typical nemaline myopathy
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare cardiac disease
- 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: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: x-linked dominant
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.