Cytoscape Web
Click node...


4 OMIM references -
1 associated gene
6 signs/symptoms
PROTEIN INTERACTIONS: 1
Chronic intestinal pseudoobstruction
Growth retardation-mild developmental delay-chronic hepatitis syndrome

FLNA SH2B3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FLNA
(0.77)
SH2B3



Citations in the biomedical literature:


Chronic intestinal pseudoobstruction
FLNA
Growth retardation-mild developmental delay-chronic hepatitis syndrome
SH2B3



Chronic intestinal pseudoobstruction
Growth retardation-mild developmental delay-chronic hepatitis syndrome

Synonym(s):
- CIPO

Synonym(s):
(no synonyms)

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

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

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive

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


Growth retardation-mild developmental delay-chronic hepatitis syndrome

(no data available)