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5 OMIM references -
3 associated genes
No signs/symptoms info
COMMON GENES: 1
4 OMIM references -
1 associated gene
6 signs/symptoms
Periventricular nodular heterotopia
Chronic intestinal pseudoobstruction

ARFGEF2 FLNA
ERMARD
FLNA


COMMON
GENES
FLNA



Citations in the biomedical literature:


Periventricular nodular heterotopia
ARFGEF2 ERMARD FLNA
Chronic intestinal pseudoobstruction



Periventricular nodular heterotopia
Chronic intestinal pseudoobstruction

Synonym(s):
(no synonyms)

Synonym(s):
- CIPO

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
(no data available)

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the digestive system -

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

External references:
5 OMIM references -
1 MeSH reference: D054091
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


Periventricular nodular heterotopia

(no data available)