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Congenital lethal myopathy, Compton-North type
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Idiopathic bronchiectasis
3 OMIM references -
4 associated genes
No signs/symptoms info
Congenital lethal myopathy, Compton-North type
Idiopathic bronchiectasis

CNTN1
(UniProt - OMIM)
 CFTR
(UniProt - OMIM)
SCNN1A
(UniProt - OMIM)
SCNN1B
(UniProt - OMIM)
SCNN1G
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CNTN1
(0.62)
SCNN1B


Citations in the biomedical literature:


Congenital lethal myopathy, Compton-North type
CNTN1
Idiopathic bronchiectasis
CFTR SCNN1A SCNN1B SCNN1G



Congenital lethal myopathy, Compton-North type
Idiopathic bronchiectasis

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare respiratory disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the respiratory system -
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:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
3 OMIM references -
No MeSH references
No signs/symptoms info available.