SCID

1000	immunodeficiency
548	autosomal
448	recessive
441	syndrome
441	mutations
437	agammaglobulinemia
427	symptoms
419	encephalopathy
418	hypogammaglobulinemia
418	deficiency

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autoimmune abnormalities severe neutropenia telangiectasia chromosome dystrophy diarrhea dysplasia congenital chromosomal tumours necrosis lymphoproliferative congenita disorder atrophy gene disorders infections Clinically infection clinically lesions tumors disease lymphoma gastrointestinal gastroenteritis anemia ataxia dysfunction arthritis fetalis allergy colitis retardation antibodies liver

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