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4 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 OMIM references -
5 associated genes
No signs/symptoms info
Severe congenital nemaline myopathy
Herpetic encephalitis

ACTA1 TBK1
KLHL40 TICAM1
KLHL41 TLR3
NEB TRAF3
UNC93B1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ACTA1
(0.52)
TRAF3



Citations in the biomedical literature:


Severe congenital nemaline myopathy
ACTA1 KLHL40 KLHL41 NEB
Herpetic encephalitis
TBK1 TICAM1 TLR3 TRAF3 UNC93B1



Severe congenital nemaline myopathy
Herpetic encephalitis

Synonym(s):
(no synonyms)

Synonym(s):
- HSV encephalitis
- Herpes simplex encephalitis
- Herpes simplex neuroinvasion

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
- Rare infectious disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
(no data available)

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: variable
Average age of death: any age
Type of inheritance: sporadic

External references:
No OMIM references
No MeSH references
External references:
4 OMIM references -
No MeSH references

No signs/symptoms info available.