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Congenital intrinsic factor deficiency
2 OMIM references -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Gräsbeck-Imerslund disease
1 OMIM reference -
2 associated genes
No signs/symptoms info
Congenital intrinsic factor deficiency
Gräsbeck-Imerslund disease

GIF
(UniProt - OMIM)
 AMN
(UniProt - OMIM)
CUBN
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
GIF
(0.88)
CUBN


Citations in the biomedical literature:


Congenital intrinsic factor deficiency
GIF
Gräsbeck-Imerslund disease
AMN CUBN



Congenital intrinsic factor deficiency
Gräsbeck-Imerslund disease

Synonym(s):
- Congenital pernicious anemia
- Gastric intrinsic factor deficiency
- Hereditary juvenile meganoblastic anemia due to intrinsic factor deficiency
- IFD
- Intrinsic factor deficiency
Synonym(s):
- Familial megaloblastic anemia
- Selective cobalamin malabsorption with proteinuria
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare hematologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare gastroenterologic disease
- Rare genetic disease
- Rare hematologic disease
- Rare renal disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.