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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
Familial hemophagocytic lymphohistiocytosis
5 OMIM references -
4 associated genes
No signs/symptoms info
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Familial hemophagocytic lymphohistiocytosis

LMNA
(UniProt - OMIM)
 PRF1
(UniProt - OMIM)
STX11
(UniProt - OMIM)
STXBP2
(UniProt - OMIM)
UNC13D
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
LMNA
(0.63)
UNC13D


Citations in the biomedical literature:


Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA
Familial hemophagocytic lymphohistiocytosis
PRF1 STX11 STXBP2 UNC13D



Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Familial hemophagocytic lymphohistiocytosis

Synonym(s):
(no synonyms)

Synonym(s):
- Familial HLH
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
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: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
5 OMIM references -
No MeSH references
No signs/symptoms info available.