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Autosomal recessive hyper-IgE syndrome
2 OMIM references -
1 associated gene
5 connected diseases
No signs/symptoms info
Disease Type of connection
Autosomal dominant nonsyndromic intellectual deficit
Combined immunodeficiency due to DOCK8 deficiency
Adams-Oliver syndrome
Pyogenic bacterial infections due to MyD88 deficiency
Waldenström macroglobulinemia
Synonym(s):
- AR-HIES
- Autosomal recessive HIES
- Hyperimmunoglobulin E syndrome type 2
- Non-skeletal hyper-IgE syndrome
Classification (Orphanet):
(no data available)
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:
2 OMIM references -
No MeSH references
Gene symbol UniProt reference OMIM reference
DOCK8 Q8NF50611432
No signs/symptoms info available.