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Congenital chronic diarrhea with protein-losing enteropathy
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial renal amyloidosis due to Apolipoprotein AI variant
1 associated gene
No signs/symptoms info
Congenital chronic diarrhea with protein-losing enteropathy
Familial renal amyloidosis due to Apolipoprotein AI variant

DGAT1
(UniProt - OMIM)
 APOA1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
DGAT1
(0.49)
APOA1


Citations in the biomedical literature:


Congenital chronic diarrhea with protein-losing enteropathy
DGAT1
Familial renal amyloidosis due to Apolipoprotein AI variant
APOA1



Congenital chronic diarrhea with protein-losing enteropathy
Familial renal amyloidosis due to Apolipoprotein AI variant

Synonym(s):
- Congenital chronic diarrhea with exudative enteropathy
Synonym(s):
- Apolipoprotein AI amyloidosis
- Familial amyloid nephropathy due to apolipoprotein AI variant
- Hereditary amyloid nephropathy due to apolipoprotein AI variant
- Hereditary renal amyloidosis due to apolipoprotein AI variant
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Certain conditions originating in the perinatal period -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.