ODCs

Click node...

5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Typical nemaline myopathy

Distal myopathy with posterior leg and anterior hand involvement


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TPM2	(0.63)	FLNC

Citations in the biomedical literature:

Typical nemaline myopathy		Distal myopathy with posterior leg and anterior hand involvement
	Synonym(s): (no synonyms)		Synonym(s): - Distal ABD-filaminopathy

	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: 1-9 / 100 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adolescence / young Average age of death: no data available Type of inheritance: autosomal dominant

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

No signs/symptoms info available.