ODCs

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1 OMIM reference -
4 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

4 OMIM references -
1 associated gene
6 signs/symptoms

Myoclonus-dystonia syndrome

Chronic intestinal pseudoobstruction


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	DRD2 DYT15	(0.89) (0.49)	FLNA FLNA

Citations in the biomedical literature:

Myoclonus-dystonia syndrome		Chronic intestinal pseudoobstruction
	Synonym(s): - Alcohol-responsive dystonia - DYT11 - Hereditary essential myoclonus - Myoclonic dystonia		Synonym(s): - CIPO

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): (no data available)

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the digestive system -

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: childhood Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 1 OMIM reference - 1 MeSH reference: C536096		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
Myoclonus-dystonia syndrome
(no data available)