Cytoscape Web
Click node...

Gräsbeck-Imerslund disease
1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary breast cancer
6 OMIM references -
4 associated genes
No signs/symptoms info
Gräsbeck-Imerslund disease
Hereditary breast cancer

AMN
(UniProt - OMIM)
 BRCA1
(UniProt - OMIM)
CUBN
(UniProt - OMIM)
 BRCA2
(UniProt - OMIM)
KLLN
(UniProt - OMIM)
XRCC2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
CUBN
(0.63)
BRCA1


Citations in the biomedical literature:


Gräsbeck-Imerslund disease
AMN CUBN
Hereditary breast cancer
BRCA1 BRCA2 KLLN XRCC2



Gräsbeck-Imerslund disease
Hereditary breast cancer

Synonym(s):
- Familial megaloblastic anemia
- Selective cobalamin malabsorption with proteinuria
Synonym(s):
- Familial breast cancer
- Familial breast carcinoma
- Hereditary breast carcinoma
Classification (Orphanet):
- Inborn errors of metabolism
- Rare gastroenterologic disease
- Rare genetic disease
- Rare hematologic disease
- Rare renal disease
Classification (Orphanet):
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare oncologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
6 OMIM references -
No MeSH references
No signs/symptoms info available.