ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

4 associated genes
No signs/symptoms info

Autosomal recessive centronuclear myopathy

Intermediate nemaline myopathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TTN TTN	(0.9) (0.63)	NEB ACTA1

Citations in the biomedical literature:

Autosomal recessive centronuclear myopathy		Intermediate nemaline myopathy
	Synonym(s): - AR-CNM		Synonym(s): (no synonyms)

	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): - Diseases of the nervous system -

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

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

No signs/symptoms info available.