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: myositis (MONDO:0021167)
Parent Node: tendinopathy (MONDO:0100010)
..Starting node ..tendinitis ()
Child Nodes:
........Achilles bursitis ()
........calcific tendinitis ()
........paratenonitis ()
........patellar tendinitis ()
........tenosynovitis ()
........tibialis tendinitis ()
Sister Nodes:
..Brown's tendon sheath syndrome ()
..tendinitis ()
..tendinosis ()
..tendon sheath disorder ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	4857
Name:	tendinitis
Definition:	Inflammation of a tendon, usually resulting from an overuse injury. It is characterized by swelling of the tendon, tenderness around the inflamed tendon, and pain while moving the affected area of the body.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	inflammation of tendon; tendon inflammation; tendonitis
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal