ODCs

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5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Typical nemaline myopathy

Congenital dyserythropoietic anemia type III


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ACTA1	(0.52)	KIF23

Citations in the biomedical literature:

Typical nemaline myopathy		Congenital dyserythropoietic anemia type III
	Synonym(s): (no synonyms)		Synonym(s): - CDA III - CDA type 3 - CDA type III - Congenital dyserythropoietic anemia type 3

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

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	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: variable Average age of death: normal 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.