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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 OMIM references -
2 associated genes
No signs/symptoms info
Hyper-IgM syndrome type 2
Familial congenital mirror movements

AICDA DCC
RAD51


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
AICDA
(0.63)
RAD51



Citations in the biomedical literature:


Hyper-IgM syndrome type 2
AICDA
Familial congenital mirror movements
DCC RAD51



Hyper-IgM syndrome type 2
Familial congenital mirror movements

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

Synonym(s):
- Familial congenital controlateral synkinesia
- Hereditary congenital controlateral synkinesia
- Hereditary congenital mirror movements
- Isolated congenital controlateral synkinesia
- Isolated congenital mirror movements

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):
(no data available)

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.