ODCs

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4 OMIM references -
1 associated gene
6 signs/symptoms

COMMON GENES: 1

5 OMIM references -
3 associated genes
No signs/symptoms info

Chronic intestinal pseudoobstruction

Periventricular nodular heterotopia

Citations in the biomedical literature:

Chronic intestinal pseudoobstruction		Periventricular nodular heterotopia
	Synonym(s): - CIPO		Synonym(s): (no synonyms)

	Classification (Orphanet): (no data available)		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic 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: - Average age of death: - Type of inheritance: autosomal recessive

	External references: 4 OMIM references - No MeSH references		External references: 5 OMIM references - 1 MeSH reference: D054091

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
Periventricular nodular heterotopia
(no data available)