MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
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granulomatous autoinflammatory syndrome (MONDO:0017955)
Parent Node:
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systemic disease (MONDO:0015938)
..Starting node
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sarcoidosis ()

       Child Nodes:
........expandcardiac sarcoidosis ()
........expandhypercalcemic sarcoidosis ()
........expandLC6fgren syndrome ()
........expandneurosarcoidosis ()
........expandpulmonary sarcoidosis ()
........expandsarcoidosis, early-onset ()
........expandskin sarcoidosis ()
........expandSS3 ()
........expanduveoparotid fever ()



 Sister Nodes: 
..expandamyloidosis (disease) ()
..expandcalciphylaxis ()
..expandcapillary leak syndrome ()
..expandconnective tissue disorder due to lysyl hydroxylase-3 deficiency ()
..expandEhlers-Danlos syndrome ()
..expandhereditary hemorrhagic telangiectasia ()
..expandhypoplasminogenemia ()
..expandKikuchi-Fujimoto disease ()
..expandKimura disease ()
..expandLangerhans cell histiocytosis ()
..expandmacrophage activation syndrome ()
..expandmalignant atrophic papulosis ()
..expandMarfan and Marfan-related disorder ()
..expandmyalgia-eosinophilia syndrome associated with tryptophan ()
..expandnon-Langerhans cell histiocytosis ()
..expandpostorgasmic illness syndrome ()
..expandprogeroid and marfanoid aspect-lipodystrophy syndrome ()
..expandretinal ischemic syndrome-digestive tract small vessel hyalinosis-diffuse cerebral calcifications syndrome ()
..expandReye syndrome ()
..expandrheumatic fever ()
..expandsarcoidosis ()
..expandsystemic autoimmune disease ()
..expandsystemic disease with cataract ()
..expandsystemic disease with skin involvement ()
..expandsystemic diseases with anterior uveitis ()
..expandsystemic diseases with panuveitis ()
..expandsystemic diseases with posterior uveitis ()
..expandTAFRO syndrome ()
..expandtempi syndrome ()
..expandunexplained long-lasting fever/inflammatory syndrome ()
..expandX-linked reticulate pigmentary disorder ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:19338
Name:sarcoidosis
Definition:Sarcoidosis is a multisystemic disorder of unknown cause characterized by the formation of immune granulomas in involved organs.
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Synonyms:benign lymphogranulomatosis of Schaumann; Besnier-Boeck-Schaumann disease; besnier-Boeck-Schaumann syndrome; Boeck sarcoid; Boeck's sarcoid; Boeck's sarcoidosis; Darier-Roussy sarcoid; lupus pernio of Besnier; lymphogranulomatosis; miliary lupoid of boeck; sarcoid; sarcoidosis
Slim Mappings:
Reference: MedGen:
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MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
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