ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

6 OMIM references -
2 associated genes
No signs/symptoms info

Autosomal recessive limb-girdle muscular dystrophy type 2J

Malignant hyperthermia

TTN	(UniProt - OMIM)		CACNA1S	(UniProt - OMIM)
			RYR1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TTN	(0.63)	RYR1

Citations in the biomedical literature:

Autosomal recessive limb-girdle muscular dystrophy type 2J		Malignant hyperthermia
	Synonym(s): - LGMD2J		Synonym(s): - Hyperthermia of anesthesia - Malignant hyperpyrexia - Pharmacogenetic myopathy of anesthesia

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

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Injury, poisoning and certain other consequences of external causes -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: normal Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 6 OMIM references - 1 MeSH reference: D008305

No signs/symptoms info available.