ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 3

5 OMIM references -
4 associated genes
3 signs/symptoms

Benign Samaritan congenital myopathy

Catecholaminergic polymorphic ventricular tachycardia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RYR1 RYR1 RYR1	(0.9) (0.73) (0.52)	TRDN RYR2 CALM1

Citations in the biomedical literature:

Benign Samaritan congenital myopathy		Catecholaminergic polymorphic ventricular tachycardia
	Synonym(s): (no synonyms)		Synonym(s): - Bidirectional tachycardia - Bidirectional tachycardia induced by catecholamine - CPVT - Double tachycardia induced by catecholamines - Malignant paroxysmal ventricular tachycardia - Multifocal ventricular premature beats - Paroxysmal ventricular fibrillation - Syncopal paroxysmal tachycardia - Syncopal tachyarythmia

	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): - Diseases of the circulatory system -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: childhood Average age of death: any age Type of inheritance: autosomal dominant

	External references: No OMIM references No MeSH references		External references: 5 OMIM references - No MeSH references

Catecholaminergic polymorphic ventricular tachycardia
	Very frequent - Cardiac rhythm disorder / arrhythmia Frequent - Dizziness Occasional - Collapse / sudden death / cardiac arrest / cardiorespiratory arrest
Benign Samaritan congenital myopathy
(no data available)