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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 acute necrotizing encephalopathy
Chronic intestinal pseudoobstruction

RANBP2 FLNA


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
RANBP2
(0.49)
FLNA



Citations in the biomedical literature:


Familial acute necrotizing encephalopathy
RANBP2
Chronic intestinal pseudoobstruction
FLNA



Familial acute necrotizing encephalopathy
Chronic intestinal pseudoobstruction

Synonym(s):
- ADANE
- Recurrent acute necrotizing encephalopathy

Synonym(s):
- CIPO

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

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

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
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 acute necrotizing encephalopathy

(no data available)