ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

4 OMIM references -
1 associated gene
6 signs/symptoms

Familial hypocalciuric hypercalcemia type 1

Chronic intestinal pseudoobstruction


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CASR	(0.89)	FLNA

Citations in the biomedical literature:

Familial hypocalciuric hypercalcemia type 1		Chronic intestinal pseudoobstruction
	Synonym(s): - FHH type 1		Synonym(s): - CIPO

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare endocrine disease - Rare genetic disease - Rare respiratory disease		Classification (Orphanet): (no data available)

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Diseases of the digestive system -

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 1 OMIM reference - 1 MeSH reference: C537145		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
Familial hypocalciuric hypercalcemia type 1
(no data available)