MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

Hello! Guest! Please Login or Register! Clinician Mode

Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

*:HP: HPO terms, ND: NAMDC terms.
Most Studied CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO

Disease Browser
Parent Node: secondary glomerular disease (MONDO:0019724)
..Starting node ..immunotactoid or fibrillary glomerulopathy ()
Child Nodes:
........immunotactoid glomerulopathy ()
........non-amyloid fibrillary glomerulopathy ()
Sister Nodes:
..AA amyloidosis ()
..AApoAIV amyloidosis ()
..adult-onset Still disease ()
..AH amyloidosis ()
..AL amyloidosis ()
..anti-glomerular basement membrane disease ()
..autoimmune interstitial lung disease-arthritis syndrome ()
..Behcet disease ()
..collagen type III glomerulopathy ()
..Cryoglobulinemic vasculitis ()
..eosinophilic granulomatosis with polyangiitis ()
..familial Mediterranean fever ()
..familial visceral amyloidosis ()
..granulomatosis with polyangiitis ()
..hypocomplementemic urticarial vasculitis ()
..IgG4-related kidney disease ()
..immunoglobulin a vasculitis ()
..immunotactoid or fibrillary glomerulopathy ()
..microscopic polyangiitis ()
..mixed connective tissue disease ()
..Muckle-Wells syndrome ()
..non-amyloid monoclonal immunoglobulin deposition disease ()
..pauci-immune glomerulonephritis ()
..polyarteritis nodosa ()
..polymyositis ()
..relapsing polychondritis ()
..Reynolds syndrome ()
..systemic lupus erythematosus (disease) ()
..systemic sclerosis ()
..Takayasu arteritis ()
..temporal arteritis ()
..thromboangiitis obliterans ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	19605
Name:	immunotactoid or fibrillary glomerulopathy
Definition:	Immunotactoid or fibrillary glomerulopathy is a group of very rare glomerular diseases, composed of immunotactoid glomerulopathy (ITG) and non-amyloid fibrillary glomerulopathy (non-amyloid FGP) (see these terms), that are characterized by mesangial deposition of monoclonal microtubular or polyclonal fibrillar deposits. Both present clinically with nephrotic range proteinuria, hematuria and renal insufficiency leading to renal failure in many cases. ITG is more likely to manifest with underlying lymphoproliferative disease, hypocomplementemia, dysproteinemia, monoclonal gammopathy or occult cryoglobulinemia. Non-amyloid FGP is 10 times more frequent than ITG.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	fibrillary glomerulonephritis and immunotactoid glomerulopathy; Immunotactoid or fibrillary glomerulonephritis
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal