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4 OMIM references -
1 associated gene
6 signs/symptoms
PROTEIN INTERACTIONS: 2
Chronic intestinal pseudoobstruction
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form

FLNA CTNNA3
DSC2
DSG2
DSP
JUP
LMNA
PKP2
RYR2
TGFB3
TMEM43
TTN


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FLNA
FLNA
(0.73)
(0.63)
LMNA
TTN



Citations in the biomedical literature:


Chronic intestinal pseudoobstruction
FLNA
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
CTNNA3 DSC2 DSG2 DSP JUP LMNA
PKP2 RYR2 TGFB3 TMEM43 TTN



Chronic intestinal pseudoobstruction
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form

Synonym(s):
- CIPO

Synonym(s):
- Familial isolated arrhythmogenic ventricular cardiomyopathy, left dominant form

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

Classification (ICD10):
- Diseases of the digestive system -
Classification (ICD10):
- Diseases of the circulatory system -

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

External references:
4 OMIM references -
No MeSH references
External references:
No 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 isolated arrhythmogenic ventricular dysplasia, left dominant form

(no data available)