ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Benign Samaritan congenital myopathy

Thyrotoxic periodic paralysis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RYR1	(0.62)	CACNA1S

Citations in the biomedical literature:

Benign Samaritan congenital myopathy		Thyrotoxic periodic paralysis
	Synonym(s): (no synonyms)		Synonym(s): - Thyrotoxic hypokalemic periodic paralysis

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare neurologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the nervous 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 / 1 000 000 Average age onset: adulthood Average age of death: normal Type of inheritance: sporadic

	External references: No OMIM references No MeSH references		External references: 3 OMIM references - No MeSH references

No signs/symptoms info available.