ODCs

Click node...

3 OMIM references -
4 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

2 OMIM references -
1 associated gene
No signs/symptoms info

Familial short QT syndrome

Rippling muscle disease


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

Citations in the biomedical literature:

Familial short QT syndrome		Rippling muscle disease
	Synonym(s): - SQTS		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare cardiac disease - Rare genetic disease		Classification (Orphanet): - Rare genetic 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: variable Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 3 OMIM references - No MeSH references		External references: 2 OMIM references - 1 MeSH reference: C535685

No signs/symptoms info available.