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Congenital chronic diarrhea with protein-losing enteropathy
1 associated gene
4 connected diseases
No signs/symptoms info
Disease Type of connection
Apolipoprotein A-I deficiency
Familial renal amyloidosis due to Apolipoprotein AI variant
Familial renal amyloidosis due to Apolipoprotein AII variant
Primary systemic amyloidosis
Synonym(s):
- Congenital chronic diarrhea with exudative enteropathy
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
Classification (ICD10):
- Certain conditions originating in the perinatal period -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
DGAT1 O75907604900
No signs/symptoms info available.