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Acute encephalopathy with biphasic seizures and late reduced diffusion
1 associated gene
7 connected diseases
No signs/symptoms info
Disease Type of connection
Myoclonus-dystonia syndrome
Autosomal dominant macrothrombocytopenia
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Familial isolated dilated cardiomyopathy
Omenn syndrome
Severe combined immunodeficiency due to adenosine deaminase deficiency
Catecholaminergic polymorphic ventricular tachycardia
Synonym(s):
- AESD
- AIEF
- Acute infantile encephalopathy predominantly affecting the frontal lobes
Classification (Orphanet):
- Rare neurologic disease
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
ADORA2A P29274102776
No signs/symptoms info available.