ODCs

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

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

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

Autosomal dominant centronuclear myopathy

Malignant hyperthermia


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

Citations in the biomedical literature:

Autosomal dominant centronuclear myopathy		Malignant hyperthermia
	Synonym(s): - AD-CNM		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: Class of prevalence: unknown Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: normal Type of inheritance: autosomal dominant

	External references: 2 OMIM references - No MeSH references		External references: 6 OMIM references - 1 MeSH reference: D008305

No signs/symptoms info available.