MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

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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)
Parent Node: serositis (MONDO:0043786)
Parent Node: synovium disease (MONDO:0056799)
..Starting node ..synovitis (disease) ()
Child Nodes:
........gonococcal synovitis ()
........pigmented villonodular synovitis ()
Sister Nodes:
..synovial bursa disease ()
..synovial plica syndrome ()
..synovitis (disease) ()
..synovium neoplasm ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	2400
Name:	synovitis (disease)
Definition:	Inflammation of a synovial membrane.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	inflammation of synovial membrane of synovial joint; synovial membrane of synovial joint inflammation; Synovitides; synovitis
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal