4A01.34ICD-11 MMS 2026-01
Hyperimmunoglobulin E syndromes
Index terms
- Hyperimmunoglobulin E syndromes
- Buckley syndrome
- HIE - [Hyperimmunoglobulin E] syndrome
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- IgE syndromes
- Job syndrome
- Job-Buckley syndrome
- Quie-Hill syndrome
- recurring cold staphylococcal abscesses
- Autosomal dominant hyperimmunoglobulin E syndrome
- AD-HIES - [Autosomal dominant hyperimmunoglobulin E] syndrome
- Autosomal dominant hyper-IgE syndrome
- Hyperimmunoglobulin E syndrome type 1
- Hyperimmunoglobulin E-recurrent infection syndrome
- Autosomal recessive hyperimmunoglobulin E syndrome
- Autosomal recessive HIES - [Autosomal recessive hyperimmunoglobulin E] syndrome
- Autosomal recessive hyper-IgE syndrome
- Hyperimmunoglobulin E syndrome type 2
- Nonskeletal hyper IgE syndrome
- SCID - [Severe combined immunodeficiency] due to DOCK8 deficiency
- SCID - [Severe combined immunodeficiency] due to dedicator of cytokinesis 8 protein deficiency
- Hyperimmunoglobulin E syndrome due to TYK2 deficiency
Exclusions from above levels
Sibling codes
Foundation entity
Hyperimmunoglobulin E syndromes – http://id.who.int/icd/entity/223461798
Part of: 4A01.3: Other well-defined immunodeficiency syndromes due to defects in adaptive immunity › 4A01: Primary immunodeficiencies due to disorders of adaptive immunity › 04: Diseases of the immune system