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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: Fistula (D005402)
Parent Node: Vascular Diseases (D014652)
Parent Node: Vascular Malformations (D054079)
..Starting node ..Vascular Fistula (D016157)
Child Nodes:
........Arterio-Arterial Fistula (D001159) 2
........Arteriovenous Fistula (D001164) 3
Sister Nodes:
..Arterial Tortuosity Syndrome (C565942)
..Arterio-Arterial Fistula (D001159) 2
..Arteriovenous Malformations (D001165) 12
..Capillary Malformations, Congenital, 1 (C562760) 1
..Central Nervous System Vascular Malformations (D020785) 10
..Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi (C567863)
..Distichiasis with Congenital Anomalies of the Heart and Peripheral Vasculature (C565092)
..Hemophilia A with Vascular Abnormality (C564415)
..May-Thurner Syndrome (D062108)
..Patent Ductus Venosus (C562830)
..Prepapillary Vascular Loops (C563287)
..Pulmonary Atresia (D018633) 2
..Scimitar Syndrome (D012587) 1
..Single Umbilical Artery (D058529)
..Splenoportal Vascular Anomalies (C562761)
..Telangiectasia, Hereditary Hemorrhagic (D013683) 4
..Vascular Fistula (D016157) 7
..Vascular Malformation, Primary Intraosseous (C564648)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11528
Name:	Vascular Fistula
Definition:	An abnormal passage between two or more BLOOD VESSELS, between ARTERIES; VEINS; or between an artery and a vein.
Alternative IDs:
ParentIDs:	MESH:D005402\|MESH:D014652\|MESH:D054079
TreeNumbers:	C14.240.850.984 \|C14.907.933 \|C23.300.575.950
Synonyms:	Fistulas, Vascular \|Fistula, Vascular \|Vascular Fistulas
Slim Mappings:	Cardiovascular disease\|Pathology (anatomical condition)
Reference:	MedGen: D016157 MeSH: D016157 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants