The following pages link to Properdin deficiency
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (links | edit)
- Choroideremia (links | edit)
- Meningococcal disease (links | edit)
- IPEX syndrome (links | edit)
- Simpson–Golabi–Behmel syndrome (links | edit)
- Properdin (links | edit)
- Antibody-dependent cellular cytotoxicity (links | edit)
- Hyperimmunoglobulin E syndrome (links | edit)
- X-linked severe combined immunodeficiency (links | edit)
- Selective immunoglobulin A deficiency (links | edit)
- Centronuclear myopathy (links | edit)
- HIV/AIDS (links | edit)
- Oculocerebrorenal syndrome (links | edit)
- Idiopathic CD4+ lymphocytopenia (links | edit)
- ATR-X syndrome (links | edit)
- Combined immunodeficiencies (links | edit)
- Nezelof syndrome (links | edit)
- Hunter syndrome (links | edit)
- Emery–Dreifuss muscular dystrophy (links | edit)
- McLeod syndrome (links | edit)
- Partial androgen insensitivity syndrome (links | edit)
- Dysgammaglobulinemia (links | edit)
- X-linked dominant inheritance (links | edit)
- Bare lymphocyte syndrome (links | edit)
- X-linked hypophosphatemia (links | edit)
- Hypohidrotic ectodermal dysplasia (links | edit)
- Conradi–Hünermann syndrome (links | edit)
- Hyper IgM syndrome (links | edit)
- Hyper-IgM syndrome type 1 (links | edit)
- Hyper-IgM syndrome type 2 (links | edit)
- Hyper-IgM syndrome type 5 (links | edit)
- Primary immunodeficiency (links | edit)
- Craniofrontonasal dysplasia (links | edit)
- Dent's disease (links | edit)
- Purine nucleoside phosphorylase deficiency (links | edit)
- Complement deficiency (links | edit)
- WHIM syndrome (links | edit)
- Brunner syndrome (links | edit)
- Immune disorder (links | edit)
- IgG deficiency (links | edit)
- Transient hypogammaglobulinemia of infancy (links | edit)
- X-linked lymphoproliferative disease (links | edit)
- Outline of immunology (links | edit)
- Ocular albinism (links | edit)
- Isolated primary immunoglobulin M deficiency (links | edit)
- Humoral immune deficiency (links | edit)
- Orofaciodigital syndrome 1 (links | edit)
- Complement 2 deficiency (links | edit)
- Focal dermal hypoplasia (links | edit)
- CHILD syndrome (links | edit)