MSeqDR Mitochondrial disease browser phenotype pathogenic gene and mutation portal

Hello! Guest! Please Login or Register! Clinician Mode

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 ..myofascial pain syndrome ()
Child Nodes:
........temporomandibular joint dysfunction syndrome ()
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:	6862
Name:	myofascial pain syndrome
Definition:	Muscular pain in numerous body regions that can be reproduced by pressure on trigger points, localized hardenings in skeletal muscle tissue. Pain is referred to a location distant from the trigger points. A prime example is the temporomandibular joint dysfunction syndrome.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: TMEM216;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal