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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
3 OMIM references -
4 associated genes
No signs/symptoms info
Laminopathy type Decaudain-Vigouroux
Idiopathic bronchiectasis

LMNA CFTR
SCNN1A
SCNN1B
SCNN1G


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LMNA
(0.63)
CFTR



Citations in the biomedical literature:


Laminopathy type Decaudain-Vigouroux
LMNA
Idiopathic bronchiectasis
CFTR SCNN1A SCNN1B SCNN1G



Laminopathy type Decaudain-Vigouroux
Idiopathic bronchiectasis

Synonym(s):
- Laminopathy with severe metabolic syndrome and myopathy

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (Orphanet):
- Rare respiratory disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Diseases of the respiratory system -

Epidemiological data:
(no data available)
Epidemiological data:
(no data available)

External references:
No OMIM references
No MeSH references
External references:
3 OMIM references -
No MeSH references

No signs/symptoms info available.