| Disease Browser
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Parent Node:
 Urologic Diseases (D014570) |
..Starting node
.. Kidney Diseases (D007674)
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Child Nodes:
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| ........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 |
Sister Nodes: |
..Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities (C567716)
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..Kidney Diseases (D007674) 345
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..Ureteral Diseases (D014515) 6
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..Urethral Diseases (D014522) 12
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..Urinary Bladder Diseases (D001745) 23
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..Urinary Tract Infections (D014552) 3
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..Urination Disorders (D014555) 26
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..Urofacial syndrome (C536480)
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..Urolithiasis (D052878) 19
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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