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Rippling muscle disease
2 OMIM references -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial short QT syndrome
3 OMIM references -
4 associated genes
No signs/symptoms info
Rippling muscle disease
Familial short QT syndrome

CAV3
(UniProt - OMIM)
 CACNA2D1
(UniProt - OMIM)
KCNH2
(UniProt - OMIM)
KCNJ2
(UniProt - OMIM)
KCNQ1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CAV3
(0.63)
KCNH2


Citations in the biomedical literature:


Rippling muscle disease
CAV3
Familial short QT syndrome
CACNA2D1 KCNH2 KCNJ2 KCNQ1



Rippling muscle disease
Familial short QT syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- SQTS
Classification (Orphanet):
- Rare genetic 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:
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
1 MeSH reference: C535685
External references:
3 OMIM references -
No MeSH references
No signs/symptoms info available.