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4 OMIM references -
1 associated gene
6 signs/symptoms
PROTEIN INTERACTIONS: 1
4 OMIM references -
2 associated genes
1 sign/symptom
Chronic intestinal pseudoobstruction
Familial hypospadias

FLNA AR
MAMLD1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FLNA
(0.84)
AR



Citations in the biomedical literature:


Chronic intestinal pseudoobstruction
FLNA
Familial hypospadias
AR MAMLD1



Chronic intestinal pseudoobstruction
Familial hypospadias

Synonym(s):
- CIPO

Synonym(s):
(no synonyms)

Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare urogenital 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: unknown
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant

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

Chronic intestinal pseudoobstruction
Familial hypospadias

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


Very frequent
- Hypospadias / epispadias / bent penis