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Chronic intestinal pseudoobstruction
4 OMIM references -
1 associated gene
6 signs/symptoms
PROTEIN INTERACTIONS: 1
Juvenile autosomal recessive medullary cystic kidney disease
5 associated genes
No signs/symptoms info
Chronic intestinal pseudoobstruction
Juvenile autosomal recessive medullary cystic kidney disease

FLNA
(UniProt - OMIM)
 ANKS6
(UniProt - OMIM)
GLIS2
(UniProt - OMIM)
NPHP1
(UniProt - OMIM)
NPHP4
(UniProt - OMIM)
WDR19
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
FLNA
(0.87)
NPHP1


Citations in the biomedical literature:


Chronic intestinal pseudoobstruction
FLNA
Juvenile autosomal recessive medullary cystic kidney disease
ANKS6 GLIS2 NPHP1 NPHP4 WDR19



Chronic intestinal pseudoobstruction
Juvenile autosomal recessive medullary cystic kidney disease

Synonym(s):
- CIPO
Synonym(s):
(no synonyms)
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the digestive system -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: -
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


Juvenile autosomal recessive medullary cystic kidney disease

(no data available)