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:
expand
kidney neoplasm (MONDO:0021163)
Parent Node:
expand
plasma cell neoplasm (MONDO:0004959)
Parent Node:
expand
secondary glomerular disease (MONDO:0019724)
..Starting node
..expand
non-amyloid monoclonal immunoglobulin deposition disease ()

       Child Nodes:
........expandheavy chain deposition disease ()
........expandlight and heavy chain deposition disease ()
........expandlight chain deposition disease ()



 Sister Nodes: 
..expandAA amyloidosis ()
..expandAApoAIV amyloidosis ()
..expandadult-onset Still disease ()
..expandAH amyloidosis ()
..expandAL amyloidosis ()
..expandanti-glomerular basement membrane disease ()
..expandautoimmune interstitial lung disease-arthritis syndrome ()
..expandBehcet disease ()
..expandcollagen type III glomerulopathy ()
..expandCryoglobulinemic vasculitis ()
..expandeosinophilic granulomatosis with polyangiitis ()
..expandfamilial Mediterranean fever ()
..expandfamilial visceral amyloidosis ()
..expandgranulomatosis with polyangiitis ()
..expandhypocomplementemic urticarial vasculitis ()
..expandIgG4-related kidney disease ()
..expandimmunoglobulin a vasculitis ()
..expandimmunotactoid or fibrillary glomerulopathy ()
..expandmicroscopic polyangiitis ()
..expandmixed connective tissue disease ()
..expandMuckle-Wells syndrome ()
..expandnon-amyloid monoclonal immunoglobulin deposition disease ()
..expandpauci-immune glomerulonephritis ()
..expandpolyarteritis nodosa ()
..expandpolymyositis ()
..expandrelapsing polychondritis ()
..expandReynolds syndrome ()
..expandsystemic lupus erythematosus (disease) ()
..expandsystemic sclerosis ()
..expandTakayasu arteritis ()
..expandtemporal arteritis ()
..expandthromboangiitis obliterans ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:19463
Name:non-amyloid monoclonal immunoglobulin deposition disease
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:non-amyloid MIDD; Randall disease
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal