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Congenital myopathy with excess of thin filaments
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Congenital dyserythropoietic anemia type III
1 OMIM reference -
1 associated gene
No signs/symptoms info
Congenital myopathy with excess of thin filaments
Congenital dyserythropoietic anemia type III

ACTA1
(UniProt - OMIM)
 KIF23
(UniProt - OMIM)

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


Citations in the biomedical literature:


Congenital myopathy with excess of thin filaments
ACTA1
Congenital dyserythropoietic anemia type III
KIF23



Congenital myopathy with excess of thin filaments
Congenital dyserythropoietic anemia type III

Synonym(s):
- Actin myopathy
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:
(no data available)
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:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.