Disease Browser
Parent Node: Arterial Occlusive Diseases (D001157) Parent Node: Kidney Diseases (D007674) ..Starting node .. Renal Artery Obstruction (D012078) Child Nodes:
Sister Nodes: ..46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS (OMIM:611812) ..AIDS-Associated Nephropathy (D016263) ..Alsing syndrome (C536588) ..Anuria (D001002) ..Arnold Stickler Bourne syndrome (C537431) ..Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease (C565928) ..Bifid Nose With Or Without Anorectal And Renal Anomalies (C567672) ..Blue diaper syndrome (C536239) ..Complement Factor H Deficiency (C562875) ..Diabetes Insipidus (D003919) 10 ..Diabetic Nephropathies (D003928) 4 ..Dimauro disease (C536176) ..Fanconi Syndrome (D005198) 3 ..Hepatorenal Syndrome (D006530) ..Hereditary renal agenesis (C536482) ..Herrmann syndrome (C538113) ..Hydranencephaly with Renal Aplasia-Dysplasia (C565507) ..Hydronephrosis (D006869) 5 ..Hyperoxaluria (D006959) 4 ..Hypertension, Renal (D006977) 3 ..HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 1 (OMIM:162000) ..HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 3 (OMIM:614227) ..Ichthyosis, mental retardation, dwarfism, and renal impairment (C536274) ..Infundibulopelvic dysgenesis (C535528) ..Jejunal atresia with renal adysplasia (C537567) ..Joubert syndrome 5 (C537688) ..Joubert syndrome 6 (C537689) ..Joubert Syndrome 9 (C567364) ..Juvenile gout (C537696) ..Kidney Cortex Necrosis (D007673) ..Kidney Diseases, Cystic (D052177) 52 ..Kidney Neoplasms (D007680) 23 ..Kidney Papillary Necrosis (D007681) ..Lachiewicz Sibley syndrome (C538131) ..Lipoprotein Glomerulopathy (C567089) ..Lymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus (C567188) ..MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY) (OMIM:612075) ..Nephritis (D009393) 51 ..Nephrocalcinosis (D009397) 6 ..Nephrolithiasis (D053040) 11 ..NEPHRONOPHTHISIS-LIKE NEPHROPATHY 1 (OMIM:613159) ..Nephropathy with Pretibial Epidermolysis Bullosa and Deafness (C563798) ..Nephrosclerosis (D009400) ..Nephrosis (D009401) 22 ..Perinephritis (D010501) ..Radio renal syndrome (C536267) ..Ren-Related Kidney Disease (C580420) ..Renal Artery Obstruction (D012078) ..Renal dysplasia - limb defects syndrome (C537754) ..Renal Hypodysplasia, Nonsyndromic, 1 (C563661) ..Renal Insufficiency (D051437) 15 ..Renal Nutcracker Syndrome (D059228) ..Renal Osteodystrophy (D012080) ..RENAL TUBULAR DYSGENESIS (OMIM:267430) ..Renal Tubular Transport, Inborn Errors (D015499) 76 ..Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia due to Duplication of Mitochondrial DNA (C564014) ..Selig Benacerraf Greene syndrome (C535840) ..Sex Reversal, Female, With Dysgenesis Of Kidneys, Adrenals, And Lungs (C567517) ..Siegler Brewer Carey syndrome (C537335) ..Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, And Progressive Nephropathy (C566682) ..Thrombocytopenia with Elevated Serum Iga and Renal Disease (C564051) ..Thyrocerebral-retinal syndrome (C536908) ..Tuberculosis, Renal (D014398) ..Uremia (D014511) 4 ..Zellweger Syndrome (D015211) 3 Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 9646
Name: Renal Artery Obstruction
Definition: Narrowing or occlusion of the RENAL ARTERY or arteries. It is due usually to ATHEROSCLEROSIS; FIBROMUSCULAR DYSPLASIA; THROMBOSIS; EMBOLISM, or external pressure. The reduced renal perfusion can lead to renovascular hypertension (HYPERTENSION, RENOVASCULAR).
Alternative IDs:
ParentIDs: MESH:D001157|MESH:D007674
TreeNumbers: C12.777.419.775 |C13.351.968.419.775 |C14.907.137.727
Synonyms: Obstruction, Renal Artery |Obstructions, Renal Artery |Renal Artery Obstructions |Renal Artery Stenoses |Renal Artery Stenosis |Stenoses, Renal Artery |Stenosis, Renal Artery
Slim Mappings: Cardiovascular disease|Urogenital disease (female)|Urogenital disease (male)
Reference:
MedGen: D012078
MeSH: D012078
OMIM: Genes: Phenotypes Disease Causing ClinVar Variants