Immunodeficiency 42 (IMD42)

Alias:

Autosomal Recessive Mendelian Susceptibility to Mycobacterial Diseases Due to Complete Rorgamma Receptor Deficiency

Imd42

Autosomal Recessive Msmd Due to Complete Rorgamma Receptor Defiency

Autosomal Recessive Primary Immunodeficiency Due to Rorc Mutation

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Immunodeficiency 42, is also known as autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete rorgamma receptor deficiency. An important gene associated with Immunodeficiency 42 is RORC (RAR Related Orphan Receptor C). Affiliated tissues include t cells and thymus, and related phenotypes are bcgosis and chronic oral candidiasis

Related ID：

MALACARDS：IMM118

OMIM：616622

MESH：D007153