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Differential Diagnosis For Family history/Immune defects


List of current finding(s):

Congenital, Developmental Disorders
Immundeficiency, combined B And T cell
Agammaglobulinemia, congenital/autosomal
Job syndrome (Hyper IgE syndrome)
Hereditary, Familial, Genetic Disorders
Granulomatous dis/childhood, chronic
Agammaglobulinemia, x-linked, infantile
Hypogammaglobulinemia, cong. X-linked
Complement deficiency syndrome
PFAPA/Periodic fever (Marshals benign)
Wiskott-Aldrich syndrome
Complement C'3 deficiency
Dysautonomia, familial
Severe combined immunodeficiency synd/SCID
Shwachman (Shwachman-Diamond) syndrome
Vegetative, Autonomic, Endocrine Disorders
Hypogammaglobulinemia of infancy, transient
Reference to Organ System
Immunodeficiency (common variable)
Properdin deficiency
allergic/immunologic body system, allergic/immunologic organ system, body system allergic/immunologic, Defective, Family history, immune system, Immune system structure, Immune system structure (body structure), Immune Systems, immunologic/allergic organ system, organ system allergic/immunologic, Structure of immune system, Structure of immune system (body structure), System Immune, Systems Immune
External Links Related to Family history/Immune defects
PubMed (National Library of Medicine)
NGC (National Guideline Clearinghouse)
Medscape (eMedicine)
Harrison's Online (accessmedicine)
NEJM (The New England Journal of Medicine)