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Immunodeficiency due to CD25 deficiency
1 OMIM reference -
1 associated gene
7 connected diseases
No signs/symptoms info
Disease Type of connection
Juvenile rheumatoid factor-negative polyarthritis
Oligoarticular juvenile arthritis
Chronic mucocutaneous candidiasis
Acute promyelocytic leukemia
Autosomal dominant hyper-IgE syndrome
Laron syndrome with immunodeficiency
Romano-Ward syndrome
Synonym(s):
- Interleukin-2 receptor alpha chain deficiency
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
IL2RA P01589147730
No signs/symptoms info available.