ODCs

Click node...

4 OMIM references -
1 associated gene
6 signs/symptoms

COMMON GENES: 1
COMMON SIGNS: 1

2 OMIM references -
2 associated genes
8 signs/symptoms

Chronic intestinal pseudoobstruction

Congenital short bowel syndrome

FLNA	(UniProt - OMIM)		CLMP	(UniProt - OMIM)
			FLNA	(UniProt - OMIM)

Citations in the biomedical literature:

Chronic intestinal pseudoobstruction		Congenital short bowel syndrome
	Synonym(s): - CIPO		Synonym(s): (no synonyms)

	Classification (Orphanet): (no data available)		Classification (Orphanet): - Rare abdominal surgical disease - Rare developmental defect during embryogenesis - Rare gastroenterologic disease - Rare genetic 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: 2 OMIM references - No MeSH references


COMMON SIGNS	- Intestinal / gut / bowel malrotation

Chronic intestinal pseudoobstruction		Congenital short bowel syndrome
	Very frequent - Intestinal / colonic anomaly Frequent - Gastric / pyloric stenosis - Structural anomalies of the nervous system Occasional - Patent ductus arteriosus - Platelets shape anomalies		Very frequent - Short bowel Frequent - Hypotrichosis / atrichia / atrichiasis / scalp hairlessness - Intellectual deficit / mental / psychomotor retardation / learning disability - Lipoatrophy - Short stature / dwarfism / nanism - Stillbirth / neonatal death Occasional - Hypospadias / epispadias / bent penis