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: myopathy (MONDO:0005336)
..Starting node ..myositis ()
Child Nodes:
........bacterial myositis ()
........fibromyalgia ()
........fungal myositis ()
........idiopathic granulomatous myositis ()
........inclusion body myositis ()
........infectious myositis ()
........myositis fibrosa ()
........myositis ossificans ()
........orbital plasma cell granuloma ()
........polymyositis ()
........tendinitis ()
........viral myositis ()
Sister Nodes:
..acute quadriplegic myopathy ()
..congenital structural myopathy ()
..infectious, fungal or parasitic myopathy ()
..muscular atrophy ()
..muscular dystrophy ()
..myofascial pain syndrome ()
..myoglobinuria ()
..myopathy of extraocular muscle ()
..myopathy with eye involvement ()
..myopathy, lactic acidosis, and sideroblastic anemia ()
..myositis ()
..non-dystrophic myopathy ()
..polyglucosan body myopathy ()
..polymyalgia rheumatica ()
..spinal muscular atrophy ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	21167
Name:	myositis
Definition:	An inflammatory disease involving a pathogenic inflammatory response in the muscle tissue.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	inflammation of muscle tissue; inflammatory disorder of muscle; inflammatory disorder of muscle (disorder); muscle tissue inflammation
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal