Immunodeficiency 105

MONDO:0800104

Any immunodeficiency disease which the cause of the disease is a mutation in the PTPRC gene.

Also known as: IMD105, SCID, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive, severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive

2 clinical trials for this condition and its sub-types, 0 tagged with Immunodeficiency 105 itself.

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Part of

↑ Familial severe combined immunodeficiency (22)

Including sub-types (2) Tagged with Immunodeficiency 105 (0)

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