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Familial isolated restrictive cardiomyopathy
4 OMIM references -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Familial isolated restrictive cardiomyopathy
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

MYPN
(UniProt - OMIM)
 APP
(UniProt - OMIM)
TNNI3
(UniProt - OMIM)
TNNT2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
TNNT2
(0.56)
APP


Citations in the biomedical literature:


Familial isolated restrictive cardiomyopathy
MYPN TNNI3 TNNT2
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Familial isolated restrictive cardiomyopathy
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- Familial or idiopathic restrictive cardiomyopathy
Synonym(s):
- HCHWA, Flemish type
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Diseases of the circulatory system -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: variable
Average age of death: any age
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
4 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.