Immunodeficiency with Hyper-Igm, Type 5 (HIGM5)

Alias:

Hyper-Igm Syndrome Type 5

Higm5

Hyper-Igm Syndrome Due to Uracil N-Glycosylase

Hyper-Igm Syndrome Due to Ung Deficiency

Hyper-Igm Syndrome 5

Immunodeficiency with Hyper Igm Type 5

Hyper-Igm Immunodeficiency Syndrome, Type 5

Immunodeficiency, with Hyper Igm, Type 5

Immunodeficiency with Hyper Igm, Type 5

Immunodeficiency with Hyper-Igm 5

Hyper-Igm Immunodeficiency Type 5

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Immunodeficiency with Hyper-Igm, Type 5, also known as hyper-igm syndrome type 5, is related to selective ige deficiency disease and transient hypogammaglobulinemia of infancy. An important gene associated with Immunodeficiency with Hyper-Igm, Type 5 is UNG (Uracil DNA Glycosylase), and among its related pathways/superpathways are Homology Directed Repair and DNA Damage. Affiliated tissues include lymph node and lung, and related phenotypes are lymphadenopathy and decreased circulating iga level

Related ID：

MALACARDS：IMM176

OMIM：608106

MESH：D053306