CO COA COB COC COD COE COF COG COH COI COK COL COM CON COO COP COQ COR COS COT COU COV COW COX COY COZ
combined T and B cell inborn immunodeficiency
[group of rare congenital disorders characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels; it is inherited as an X-linked or autosomal recessive defect; about half of the patients with autosomal recessive SCID are deficient in the enzyme adenosine deaminase. ( CSP )]
UMLS (CSP) C0085110- Disease or Syndrome
Relation/PAR: hypoimmunity
Infant, Newborn, Diseases
inborn immunodeficiency
Infant, Newborn, Diseases
inborn immunodeficiency
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