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Cap myopathy
2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Idiopathic bronchiectasis
3 OMIM references -
4 associated genes
No signs/symptoms info
Cap myopathy
Idiopathic bronchiectasis

TPM2
(UniProt - OMIM)
 CFTR
(UniProt - OMIM)
TPM3
(UniProt - OMIM)
 SCNN1A
(UniProt - OMIM)
SCNN1B
(UniProt - OMIM)
SCNN1G
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
TPM3
(0.63)
CFTR


Citations in the biomedical literature:


Cap myopathy
TPM2 TPM3
Idiopathic bronchiectasis
CFTR SCNN1A SCNN1B SCNN1G



Cap myopathy
Idiopathic bronchiectasis

Synonym(s):
- Cap disease
Synonym(s):
(no synonyms)
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: variable
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
2 OMIM references -
No MeSH references
External references:
3 OMIM references -
No MeSH references
No signs/symptoms info available.