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 fibrosa ()
Child Nodes:
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:	4881
Name:	myositis fibrosa
Definition:	A form of myositis that is characterized by the formation of connective tissue within the muscle.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	interstitial myositis
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal