Cytoscape Web
Click node...


2 OMIM references -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 OMIM references -
5 associated genes
No signs/symptoms info
Familial infantile bilateral striatal necrosis
Herpetic encephalitis

ADAR TBK1
MT-ATP6 TICAM1
NUP62 TLR3
TRAF3
UNC93B1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
NUP62
(0.77)
TRAF3



Citations in the biomedical literature:


Familial infantile bilateral striatal necrosis
ADAR MT-ATP6 NUP62
Herpetic encephalitis
TBK1 TICAM1 TLR3 TRAF3 UNC93B1



Familial infantile bilateral striatal necrosis
Herpetic encephalitis

Synonym(s):
- Familial IBSN
- Familial infantile striatonigral degeneration
- Familial infantile striatonigral necrosis

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: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: any age
Type of inheritance: sporadic

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

No signs/symptoms info available.