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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 OMIM references -
1 associated gene
6 signs/symptoms
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Chronic intestinal pseudoobstruction

LMNA FLNA


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
LMNA
(0.73)
FLNA



Citations in the biomedical literature:


Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
LMNA
Chronic intestinal pseudoobstruction
FLNA



Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
Chronic intestinal pseudoobstruction

Synonym(s):
(no synonyms)

Synonym(s):
- CIPO

Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
Classification (Orphanet):
(no data available)

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the digestive system -

Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
4 OMIM references -
No MeSH references

Chronic intestinal pseudoobstruction

Very frequent
- Intestinal / colonic anomaly

Frequent
- Gastric / pyloric stenosis
- Intestinal / gut / bowel malrotation
- Structural anomalies of the nervous system

Occasional
- Patent ductus arteriosus
- Platelets shape anomalies


Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

(no data available)