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 ..crystal arthropathy ()
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:	22208
Name:	crystal arthropathy
Definition:
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	Arthritides, Crystal; Arthritides, Crystalline; Arthritis, Crystal; Arthritis, Crystalline; Arthropathies, Crystal; Arthropathies, Crystalline; Arthropathy, Crystal; Arthropathy, Crystalline; Crystal Arthritides; Crystal Arthritis; Crystal Arthropathies; Crystal Arthropathy; Crystal arthropathy; cry
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal