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Familial hypospadias

4 OMIM references -
2 associated genes
1 sign/symptom

PROTEIN INTERACTIONS: 1

Chronic intestinal pseudoobstruction

4 OMIM references -
1 associated gene
6 signs/symptoms

Familial hypospadias

Chronic intestinal pseudoobstruction

AR	(UniProt - OMIM)		FLNA	(UniProt - OMIM)
MAMLD1	(UniProt - OMIM)


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

Citations in the biomedical literature:

Familial hypospadias		Chronic intestinal pseudoobstruction
	Synonym(s): (no synonyms)		Synonym(s): - CIPO

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare urogenital 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: normal Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

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

Familial hypospadias		Chronic intestinal pseudoobstruction
	Very frequent - Hypospadias / epispadias / bent penis		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