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: limb disorder (MONDO:0044967)
Parent Node: thrombophlebitis (MONDO:0002800)
..Starting node ..femoral vein thrombophlebitis ()
Child Nodes:
Sister Nodes:
..femoral vein thrombophlebitis ()
..iliac vein thrombophlebitis ()
..thrombophlebitis migrans ()
MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD

Term ID:	1481
Name:	femoral vein thrombophlebitis
Definition:	A thrombophlebitis that involves the femoral vein.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:	femoral vein thrombophlebitis; phlebitis and thrombophlebitis of femoral vein; phlebitis and thrombophlebitis of femoral vein (deep) (superficial); thrombophlebitis of deep femoral vein; thrombophlebitis of femoral vein; thrombophlebitis of the femoral vein
Slim Mappings:
Reference:	MedGen: MeSH: OMIM: MSeqDR : Genes: RAD51C;
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal