Severe combined immunodeficiency

MONDO:0015974

Severe combined immunodeficiency (SCID) comprises a group of rare monogenic primary immunodeficiency disorders characterized by a lack of functional peripheral T lymphocytes resulting in early-onset severe respiratory infections and failure to thrive. They are classified according to immunological phenotype into SCID with absence of T cells but presence of B cells (T-B+ SCID) or SCID with absence of both (T-B- SCID). Both of these groups include several forms, with or without natural killer (NK) cells.

Also known as: SCID, severe combined immunodeficiency, severe combined immunodeficiency (disease), severe combined immunodeficiency disease

38 clinical trials for this condition and its sub-types, 24 tagged with Severe combined immunodeficiency itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Sub-types of Severe combined immunodeficiency

Most studied deeper sub-types

Sort by