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4 associated genes
No signs/symptoms info
COMMON GENES: 3
PROTEIN INTERACTIONS: 1
5 associated genes
No signs/symptoms info
Severe congenital nemaline myopathy
Typical nemaline myopathy

ACTA1 ACTA1
KLHL40 CFL2
KLHL41 KLHL41
NEB NEB
TPM2


COMMON
GENES
ACTA1
KLHL41
NEB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ACTA1
(0.56)
TPM2



Citations in the biomedical literature:


Severe congenital nemaline myopathy
ACTA1 KLHL40 KLHL41 NEB
Typical nemaline myopathy
CFL2 TPM2



Severe congenital nemaline myopathy
Typical 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: neonatal/infancy
Average age of death: child / adolescent
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: normal
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.