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: arthritis (MONDO:0005578)
..Starting node ..reactive arthritis ()
Child Nodes:
Sister Nodes:
..acute articular rheumatism ()
..adult-onset Still disease ()
..chondrocalcinosis ()
..discitis ()
..hemophilic arthropathy ()
..infective arthritis ()
..juvenile idiopathic arthritis ()
..negative rheumatoid factor polyarthritis ()
..osteoarthritis ()
..periarthritis ()
..polyarticular arthritis ()
..reactive arthritis ()
..rheumatoid arthritis ()
..synovitis (disease) ()
..transient arthritis ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	17376
Name:	reactive arthritis
Definition:	Reactive arthritis (ReA) is an autoimmune disorder belonging to the group of seronegative spondyloarthropathies and is characterized by the classic triad of arthritis, urethritis and conjunctivitis.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	arthritis urethritica; Fiessinger Leroy Reiter syndrome; Fiessinger-Leroy disease; Fiessinger-Leroy-Reiter syndrome; PIRA; polyarthritis enterica; post-bacterial arthropathy; post-infectious arthritis; post-infectious reactive arthropathy; postdysenteric arthropathy; reactive arthritis; Reiter disea
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal