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Axenfeld anomaly
2 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Chronic intestinal pseudoobstruction
4 OMIM references -
1 associated gene
6 signs/symptoms
Axenfeld anomaly
Chronic intestinal pseudoobstruction

FOXC1
(UniProt - OMIM)
 FLNA
(UniProt - OMIM)
PITX2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
FOXC1
(0.75)
FLNA


Citations in the biomedical literature:


Axenfeld anomaly
FOXC1 PITX2
Chronic intestinal pseudoobstruction
FLNA



Axenfeld anomaly
Chronic intestinal pseudoobstruction

Synonym(s):
(no synonyms)

Synonym(s):
- CIPO
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
Classification (Orphanet):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the digestive system -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
2 OMIM references -
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


Axenfeld anomaly

(no data available)