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Severe combined immunodeficiency due to adenosine deaminase deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Acute encephalopathy with biphasic seizures and late reduced diffusion
1 associated gene
No signs/symptoms info
Severe combined immunodeficiency due to adenosine deaminase deficiency
Acute encephalopathy with biphasic seizures and late reduced diffusion

ADA
(UniProt - OMIM)
 ADORA2A
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ADA
(0.83)
ADORA2A


Citations in the biomedical literature:


Severe combined immunodeficiency due to adenosine deaminase deficiency
ADA
Acute encephalopathy with biphasic seizures and late reduced diffusion
ADORA2A



Severe combined immunodeficiency due to adenosine deaminase deficiency
Acute encephalopathy with biphasic seizures and late reduced diffusion

Synonym(s):
- ADA deficiency
- SCID due to adenosine deaminase deficiency
Synonym(s):
- AESD
- AIEF
- Acute infantile encephalopathy predominantly affecting the frontal lobes
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- 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:
Class of prevalence: 1-9 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: C531816
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.