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: myositis (MONDO:0021167)
..Starting node ..myositis ossificans ()
Child Nodes:
........traumatic myositis ossificans ()
Sister 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 ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	3964
Name:	myositis ossificans
Definition:	A disorder characterized by non-neoplastic bone formation in soft tissues. It usually follows blunt trauma and bleeding in the deep soft tissues.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	fibrodysplasia ossificans progressiva; fop; Myisitis ossificans; myositis ossificans progressiva; ossification - muscle; progressive myositis ossificans; progressive ossifying myositis
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal