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

ACTA1 DMD
KLHL40
KLHL41
NEB


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Severe congenital nemaline myopathy
ACTA1 KLHL40 KLHL41 NEB
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers
DMD



Severe congenital 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 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: child / adolescent
Type of inheritance: autosomal recessive
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.