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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

Disease Browser
Parent Node: Muscular Diseases (D009135)
Parent Node: Tendon Injuries (D013708)
..Starting node ..Tendinopathy (D052256)
Child Nodes:
........Tenosynovitis (D013717) 4
Sister Nodes:
..Tendinopathy (D052256) 5
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	10915
Name:	Tendinopathy
Definition:	Clinical syndrome describing overuse tendon injuries characterized by a combination of PAIN, diffuse or localized swelling, and impaired performance. Distinguishing tendinosis from tendinitis is clinically difficult and can be made only after histopathological examination.
Alternative IDs:
ParentIDs:	MESH:D009135\|MESH:D013708
TreeNumbers:	C05.651.869 \|C26.874.800
Synonyms:	Tendinitides \|Tendinitis \|Tendinopathies \|Tendinoses \|Tendinosis \|Tendonitides \|Tendonitis
Slim Mappings:	Musculoskeletal disease\|Wounds and injuries
Reference:	MedGen: D052256 MeSH: D052256 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants