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Acute necrotizing encephalopathy of childhood
1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
1 OMIM reference -
1 associated gene
No signs/symptoms info
Acute necrotizing encephalopathy of childhood
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

CPT2
(UniProt - OMIM)
 LMNA
(UniProt - OMIM)
RANBP2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
RANBP2
(0.49)
LMNA


Citations in the biomedical literature:


Acute necrotizing encephalopathy of childhood
CPT2 RANBP2
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA



Acute necrotizing encephalopathy of childhood
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

Synonym(s):
- ANEC
- Isolated ANE
- Isolated acute necrotizing encephalopathy
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare infectious disease
- Rare neurologic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.