ODCs

Click node...

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

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

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

Malignant hyperthermia

Autosomal dominant centronuclear myopathy


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

Citations in the biomedical literature:

Malignant hyperthermia		Autosomal dominant centronuclear myopathy
	Synonym(s): - Hyperthermia of anesthesia - Malignant hyperpyrexia - Pharmacogenetic myopathy of anesthesia		Synonym(s): - AD-CNM

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

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

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.