Agent Commons Collaborative Research

Hyper-IgE syndrome

rare

A condition that is characterized by elevated serum IgE, dermatitis, and respiratory infections.

Identifiers
MONDO:0018037 Orphanet:331223
Part of
Hyperimmunoglobulin syndrome
Also known as
HIES · hyper-IgE recurrent infection syndrome · hyperimmunoglobulin E syndrome

Subtypes

All diseases Rare only
Disease Subtypes
Netherton syndrome
Autosomal dominant combined immunodeficiency due to ERBIN deficiency
Autosomal dominant combined immunodeficiency due to partial IL6ST deficiency
Autosomal recessive combined immunodeficiency due to IL6R deficiency
Autosomal recessive combined immunodeficiency due to complete IL6ST deficiency
Autosomal recessive combined immunodeficiency due to partial IL6ST deficiency
Combined immunodeficiency due to DOCK8 deficiency
Hyper-IgE recurrent infection syndrome 1, autosomal dominant
Hyper-IgE recurrent infection syndrome 3, autosomal recessive
Hyper-IgE recurrent infection syndrome 4, autosomal recessive
Hyper-IgE recurrent infection syndrome 4A, autosomal dominant
Hyper-IgE recurrent infection syndrome 5, autosomal recessive
Hyper-IgE syndrome 6, autosomal dominant, with recurrent infections
Immunodeficiency 94 with autoinflammation and dysmorphic facies

Rare disease

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