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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

Disease Browser
Parent Node: Venous Insufficiency (D014689)
..Starting node ..Venular Insufficiency, Systemic (C566004)
Child Nodes:
Sister Nodes:
..Postphlebitic Syndrome (D011186)
..Postthrombotic Syndrome (D054070)
..Venular Insufficiency, Systemic (C566004)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:

11577

Name:

Venular Insufficiency, Systemic

Definition:

Alternative IDs:

ParentIDs:

MESH:D014689

TreeNumbers:

C14.907.952/C566004

Synonyms:

Slim Mappings:

Cardiovascular disease

Reference:

MedGen: C566004
MeSH: C566004
OMIM: 192700;

Genes:

Phenotypes

1	HP:0001626	Abnormality of the cardiovascular system
2	HP:0000961	Cyanosis

Disease Causing ClinVar Variants