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: compartment syndrome (MONDO:0004001)
Parent Node: muscular disease (MONDO:0005218)
..Starting node ..anterior compartment syndrome ()
Child Nodes:
Sister Nodes:
..anterior compartment syndrome ()
..biliary dyskinesia ()
..contracture ()
..frozen shoulder ()
..Kocher-debre-Semelaigne syndrome ()
..levator syndrome ()
..muscle tissue disease ()
..myalgic encephalomeyelitis/chronic fatigue syndrome ()
..rhabdomyolysis (disease) ()
..rotator cuff syndrome ()
..sarcopenia ()
..urethral intrinsic sphincter deficiency ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	6648
Name:	anterior compartment syndrome
Definition:	Rapid swelling, increased tension, pain, and ischemic necrosis of the muscles of the anterior tibial compartment of the leg, often following excessive physical exertion.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	anterior compartment syndrome
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: MANBA;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal