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

DGAT1 APOA1


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.