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Hyper-IgM syndrome type 5
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hyper-IgM syndrome type 5
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

UNG
(UniProt - OMIM)
 APP
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
UNG
(0.56)
APP


Citations in the biomedical literature:


Hyper-IgM syndrome type 5
UNG
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
APP



Hyper-IgM syndrome type 5
Hereditary cerebral hemorrhage with amyloidosis, Flemish type

Synonym(s):
- HIGM5
- Hyper-IgM syndrome due to UNG deficiency
- Hyper-IgM syndrome due to uracil N-glycosylase
Synonym(s):
- HCHWA, Flemish type
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.