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Hyper-IgM syndrome type 5
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant Charcot-Marie-Tooth disease type 2F
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hyper-IgM syndrome type 5
Autosomal dominant Charcot-Marie-Tooth disease type 2F

UNG
(UniProt - OMIM)
 HSPB1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
UNG
(0.68)
HSPB1


Citations in the biomedical literature:


Hyper-IgM syndrome type 5
UNG
Autosomal dominant Charcot-Marie-Tooth disease type 2F
HSPB1



Hyper-IgM syndrome type 5
Autosomal dominant Charcot-Marie-Tooth disease type 2F

Synonym(s):
- HIGM5
- Hyper-IgM syndrome due to UNG deficiency
- Hyper-IgM syndrome due to uracil N-glycosylase
Synonym(s):
- CMT2F
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 / 1 000 000
Average age onset: adolescence / young
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.