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)
..Starting node ..infective arthritis ()
Child Nodes:
........bacterial arthritis ()
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:	42485
Name:	infective arthritis
Definition:	The inflammation of one or more joints caused by any infectious pathogen within the joint space. Symptoms include pain, stiffness, and decreased range of motion in the affected joint.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	infective arthritis; septic arthritis
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal