n14129351
type | n |
lex_filenum | 26 |
def | 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 |
Outgoing links | |
Hypernym | severe combined immunodeficiency, severe combined immunodeficiency disease, SCID |
Incoming links | |
Hyponym | severe combined immunodeficiency, severe combined immunodeficiency disease, SCID |
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