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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
16 OMIM references -
4 associated genes
No signs/symptoms info
Hyper-IgM syndrome type 2
Early-onset autosomal dominant Alzheimer disease

AICDA APP
PSEN1
PSEN2
SORL1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
AICDA
(0.56)
APP



Citations in the biomedical literature:


Hyper-IgM syndrome type 2
AICDA
Early-onset autosomal dominant Alzheimer disease
APP PSEN1 PSEN2 SORL1



Hyper-IgM syndrome type 2
Early-onset autosomal dominant Alzheimer disease

Synonym(s):
- AID deficiency
- Activation-induced cytidine deaminase deficiency
- HIGM2

Synonym(s):
- EOFAD
- Early-onset familial autosomal dominant Alzheimer disease
- Familial Alzheimer disease

Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: adult
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
16 OMIM references -
No MeSH references

No signs/symptoms info available.