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 ..transient arthropathy ()
Child Nodes:
........transient arthritis ()
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:	1429
Name:	transient arthropathy
Definition:	Arthropathy that is not permanent.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	transient arthropathy involving forearm; transient arthropathy involving hand; transient arthropathy involving lower leg; transient arthropathy involving multiple sites; transient arthropathy involving pelvic region and thigh; transient arthropathy involving shoulder region; transient arthropathy in
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal