Cytoscape Web
Click node...

Congenital myopathy, Paradas type
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant Charcot-Marie-Tooth disease type 2A1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Congenital myopathy, Paradas type
Autosomal dominant Charcot-Marie-Tooth disease type 2A1

DYSF
(UniProt - OMIM)
 KIF1B
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
DYSF
(0.65)
KIF1B


Citations in the biomedical literature:


Congenital myopathy, Paradas type
DYSF
Autosomal dominant Charcot-Marie-Tooth disease type 2A1
KIF1B



Congenital myopathy, Paradas type
Autosomal dominant Charcot-Marie-Tooth disease type 2A1

Synonym(s):
(no synonyms)

Synonym(s):
- CMT2A1
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:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: childhood
Average age of death: -
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.