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Familial acute necrotizing encephalopathy
1 OMIM reference -
1 associated gene
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
Familial acute necrotizing encephalopathy
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

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

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


Citations in the biomedical literature:


Familial acute necrotizing encephalopathy
RANBP2
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA



Familial acute necrotizing encephalopathy
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

Synonym(s):
- ADANE
- Recurrent acute necrotizing encephalopathy
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (ICD10):
(no data available)
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: -
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.