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Syndactyly type 3

1 OMIM reference -
1 associated gene
4 signs/symptoms

PROTEIN INTERACTIONS: 1

Chronic intestinal pseudoobstruction

4 OMIM references -
1 associated gene
6 signs/symptoms

Syndactyly type 3

Chronic intestinal pseudoobstruction

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GJA1	(0.63)	FLNA

Citations in the biomedical literature:

Syndactyly type 3		Chronic intestinal pseudoobstruction
	Synonym(s): - SD3 - Syndactyly of fingers 4 and 5		Synonym(s): - CIPO

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

	External references: 1 OMIM reference - 1 MeSH reference: C538154		External references: 4 OMIM references - No MeSH references

Syndactyly type 3		Chronic intestinal pseudoobstruction
	Very frequent - Autosomal dominant inheritance - Syndactyly of fingers / interdigital palm Frequent - Camptodactyly of some fingers Occasional - Short foot / brachydactyly of toes		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