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4 associated genes
No signs/symptoms info
COMMON GENES: 3
PROTEIN INTERACTIONS: 2
6 associated genes
No signs/symptoms info
Severe congenital nemaline myopathy
Childhood-onset nemaline myopathy

ACTA1 ACTA1
KLHL40 KBTBD13
KLHL41 KLHL41
NEB NEB
TPM2
TPM3


COMMON
GENES
ACTA1
KLHL41
NEB


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ACTA1
ACTA1
(0.65)
(0.56)
TPM3
TPM2



Citations in the biomedical literature:


Severe congenital nemaline myopathy
ACTA1 KLHL40 KLHL41 NEB
Childhood-onset nemaline myopathy
KBTBD13 TPM2 TPM3



Severe congenital nemaline myopathy
Childhood-onset nemaline myopathy

Synonym(s):
(no synonyms)

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: neonatal/infancy
Average age of death: child / adolescent
Type of inheritance: autosomal recessive
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.