Cytoscape Web
Click node...

Congenital lethal myopathy, Compton-North type
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Intellectual deficiency - hypotonia - spasticity - sleep disorder
1 OMIM reference -
1 associated gene
No signs/symptoms info
Congenital lethal myopathy, Compton-North type
Intellectual deficiency - hypotonia - spasticity - sleep disorder

CNTN1
(UniProt - OMIM)
 ANK3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CNTN1
(0.72)
ANK3


Citations in the biomedical literature:


Congenital lethal myopathy, Compton-North type
CNTN1
Intellectual deficiency - hypotonia - spasticity - sleep disorder
ANK3



Congenital lethal myopathy, Compton-North type
Intellectual deficiency - hypotonia - spasticity - sleep disorder

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):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.