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: arthropathy (MONDO:0006816)
Parent Node: tendinitis (MONDO:0004857)
Parent Node: tendon sheath disorder (MONDO:0024876)
..Starting node ..tenosynovitis ()
Child Nodes:
........bicipital tenosynovitis ()
........tenosynovitis of foot and ankle ()
Sister Nodes:
..tendon sheath fibroma ()
..tendon sheath lipoma ()
..tenosynovial giant cell tumor ()
..tenosynovitis ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	4855
Name:	tenosynovitis
Definition:	Inflammation of the synovial lining of a tendon sheath. Causes include trauma, tendon stress, bacterial disease (gonorrhea, tuberculosis), rheumatic disease, and gout. Common sites are the hand, wrist, shoulder capsule, hip capsule, hamstring muscles, and Achilles tendon. The tendon sheaths become inflamed and painful, and accumulate fluid. Joint mobility is usually reduced.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	Inflammation of tendon sheath; inflammation of tendon sheath; tendon sheath inflammation; Tenosynovitides
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal