1. (noun) SCID in male children resulting from mutation of a gene that codes for a protein on the surface of T cells that allows them to develop a growth factor receptor

• x-linked scid

1. (noun) SCID in male children resulting from mutation of a gene that codes for a protein on the surface of T cells that allows them to develop a growth factor receptor

• scid
• severe combined immunodeficiency
• severe combined immunodeficiency disease