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)
..Starting node ..de Quervain disease ()
Child Nodes:
Sister Nodes:
..ankylosis (disease) ()
..arthritis ()
..articular cartilage disease ()
..Behcet syndrome arthropathy ()
..Borrone di Rocco Crovato syndrome ()
..bursitis ()
..crystal arthropathy ()
..de Quervain disease ()
..ganglion or cyst of synovium/tendon/bursa ()
..hemarthrosis ()
..hydrarthrosis ()
..hypermobility syndrome ()
..neurogenic arthropathy ()
..patellofemoral pain syndrome ()
..secondary hypertrophic osteoarthropathy ()
..shoulder impingement syndrome ()
..spondyloarthropathy ()
..synovial plica syndrome ()
..synovium neoplasm ()
..temporomandibular joint disorder ()
..tenosynovitis ()
..Tietze syndrome ()
..transient arthropathy ()
..vertebral joint disease ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	6721
Name:	de Quervain disease
Definition:	Stenosing tenosynovitis of the abductor pollicis longus and extensor pollicis brevis tendons in the first dorsal wrist compartment. The presenting symptoms are usually pain and tenderness at the radial styloid. The cause is almost always related to overuse injury or is associated with rheumatoid arthritis.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	radial styloid tenosynovitis; tenosynovitis, de Quervain's
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
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