Immunodeficiency with Hyper-Igm, Type 4 (HIGM4)

Alias:
Hyper-Igm Syndrome Type 4
Higm4
Immunodeficiency with Hyper-Igm Type 4
Immunodeficiency, with Hyper Igm, Type 4
Hyper-Igm Syndrome 4
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Immunodeficiency with Hyper-Igm, Type 4, also known as hyper-igm syndrome type 4, is related to immunodeficiency with hyper-igm, type 3 and autoimmune lymphoproliferative syndrome. An important gene associated with Immunodeficiency with Hyper-Igm, Type 4 is UNG (Uracil DNA Glycosylase), and among its related pathways/superpathways are ERK Signaling and MIF Mediated Glucocorticoid Regulation. Affiliated tissues include lymph node, and related phenotypes are immunodeficiency and recurrent upper respiratory tract infections

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Unknown
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8
91
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Medical Symptom

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Gene & Mutation

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Disease Model

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MGI
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References Literature

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