ACTINIC PRURIGOPOLYMORPHIC LIGHT ERUPTION, HEREDITARY
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(OMIM:174770)
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Alport syndrome
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(Orphanet:63)
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Anti-glomerular basement membrane disease
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(Orphanet:375)
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C3 glomerulonephritis
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(Orphanet:329931)
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COMPLEMENT COMPONENT 4A DEFICIENCY
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(OMIM:614380)
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Eosinophilic granulomatosis with polyangiitis
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(Orphanet:183)
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Immunodeficiency with factor I anomaly
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(Orphanet:200418)
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LYMPHOPENIC HYPERGAMMAGLOBULINEMIA, ANTIBODY DEFICIENCY, AUTOIMMUNEHEMOLYTIC ANEMIA, AND GLOMERULONEPHRITIS
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(OMIM:247800)
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Microcephaly - glomerulonephritis - marfanoid habitus
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(Orphanet:2172)
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Nail-patella syndrome
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(Orphanet:2614)
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Pediatric systemic lupus erythematosus
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(Orphanet:93552)
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THROMBOCYTOPENIA WITH ELEVATED SERUM IgA AND RENAL DISEASE
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(OMIM:314000)
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Tubulointerstitial nephritis and uveitis syndrome
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(Orphanet:91500)
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