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4 OMIM references -
1 associated gene
6 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Chronic intestinal pseudoobstruction
Von Willebrand disease, platelet type

FLNA GP1BA


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FLNA
(0.73)
GP1BA



Citations in the biomedical literature:


Chronic intestinal pseudoobstruction
FLNA
Von Willebrand disease, platelet type
GP1BA



Chronic intestinal pseudoobstruction
Von Willebrand disease, platelet type

Synonym(s):
- CIPO

Synonym(s):
- PT-VWD
- Pseudo-Von Willebrand disease
- Pseudo-Von Willebrand disease type 2B

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

Classification (ICD10):
- Diseases of the digestive system -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

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

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


Von Willebrand disease, platelet type

(no data available)