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: tendinopathy (MONDO:0100010)
..Starting node ..tendon sheath disorder ()
Child Nodes:
........tendon sheath fibroma ()
........tendon sheath lipoma ()
........tenosynovial giant cell tumor ()
........tenosynovitis ()
Sister Nodes:
..Brown's tendon sheath syndrome ()
..tendinitis ()
..tendinosis ()
..tendon sheath disorder ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	24876
Name:	tendon sheath disorder
Definition:	A disease that involves the tendon sheath.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	disease of tendon sheath; disease or disorder of tendon sheath; disorder of tendon sheath; disorder of tendon sheath; tendon sheath disease; tendon sheath disease or disorder; tendon sheath disorder
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal