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:
expandscleral disease (MONDO:0001269)
..Starting node
..expandscleritis (disease) ()

       Child Nodes:
........expandanterior scleritis ()
........expandnecrotizing scleritis ()
........expandpanophthalmitis ()
........expandposterior scleritis ()
........expandscleroperikeratitis ()



 Sister Nodes: 
..expandepiscleritis periodica fugax ()
..expandnodular episcleritis ()
..expandscleral staphyloma (disease) ()
..expandscleritis (disease) ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:1718
Name:scleritis (disease)
Definition:Inflammation of the sclera.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:scleritis
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes: DES;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal