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

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

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


Citations in the biomedical literature:


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



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

Synonym(s):
(no synonyms)

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