Term Name: severe combined immunodeficiency
Synonyms: combined T and B cell inborn immunodeficiency, SCID
Definition: A combined T cell and B cell immunodeficiency that is caused by a defect in infection-fighting immune cells resulting in individuals with non-functional immune systems.
Ontology: Human Disease [DOID:627]   ( DOID:627 )

Relationships
is a type of: combined immunodeficiency
has subtype: adenosine deaminase deficiency CD3delta deficiency CD3epsilon deficiency CD3gamma deficiency CD3zeta deficiency CD45 deficiency coronin-1A deficiency immunodeficiency 11A immunodeficiency 15B immunodeficiency 19 immunodeficiency 22 immunodeficiency 24 immunodeficiency 26 janus kinase-3 deficiency MHC class I deficiency MHC class II deficiency Omenn syndrome recombinase activating gene 1 deficiency recombinase activating gene 2 deficiency reticular dysgenesis severe combined immunodeficiency with sensitivity to ionizing radiation severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive T-cell immunodeficiency, congenital alopecia, and nail dystrophy X-linked severe combined immunodeficiency