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PedAM

Pediatric Disease Annotations & Medicines




Disease severe combined immunodeficiency
Phenotype C0085110|severe combined immunodeficiency syndrome
Sentences 2
PubMedID- 21695116 A variety of mutations are responsible for the scid (severe combined immunodeficiency syndrome) phenotype with a deficiency in different lymphoid cell populations [1].
PubMedID- 23122694 Characterised traits range from severe combined immunodeficiency syndromes, with specific defects in cellular and humoral immunity, to defects in innate immunity such as impaired tlr signalling (box 1, figure 2).

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