Category:Blau syndrome

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<nowiki>Síndrome de Blau; syndrome de Blau; Zespół Blaua; Нәселле ювениль системалы гранулематоз синдромы; Síndrome de Blau; Blau-Syndrom; Blaun oireyhtymä; Blau syndrome; متلازمة بلاو; Blauov sindrom; Blauov sindrom; avtosomno dominantna bolezen, za katero so značilni družinski granulomatozni artritis, uveitis in kožni granulomi; seltene Erbkrankheit; An autosomal dominant disease characterized by familial granulomatous arthritis, uveitis and skin granulomas. It has material basis in mutations in the NOD2/CARD15 genes.; rzadkie, genetycznie uwarunkowane schorzenie; maladie rare; ARTHROCUTANEOUVEAL GRANULOMATOSIS; Jabs syndrome; Granulomatous arthritis of childhood; Synovitis granulomatous with uveitis and cranial neuropathies; Granulomatous Inflammatory Arthritis, Dermatitis, and Uveitis, Familial; ACUG; Pediatric Granulomatous Arthritis; Granulomatosis, Familial, Blau Type; BLAU SYNDROME; BLAUS; Synovitis, Granulomatous, With Uveitis and Cranial Neuropathies; BLAUS; Granulomatosis, Familial Juvenile Systemic; BLAU SYNDROME; Zespół Jabsa; arthrite pédiatrique de Granulomatous; sarcoïdose juvénile; Sindrome de Blau</nowiki>
Blau syndrome 
An autosomal dominant disease characterized by familial granulomatous arthritis, uveitis and skin granulomas. It has material basis in mutations in the NOD2/CARD15 genes.
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Instance of
  • designated intractable/rare disease
  • rare disease
  • class of disease
Subclass of
  • autosomal dominant disease
  • periodic fever syndrome
  • rare genetic eye disease
  • secondary interstitial lung disease specific to childhood associated with a granulomatous disease
  • systemic diseases with panuveitis
  • systemic diseases with anterior uveitis
  • autoinflammatory syndrome with skin involvement
  • autoinflammatory syndrome with immune deficiency
  • rare genetic respiratory disease
  • granulomatous autoinflammatory syndrome
  • syndrome
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Media in category "Blau syndrome"

The following 2 files are in this category, out of 2 total.