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

16 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by