| Disease Browser
|
Parent Node:
 Amino Acid Metabolism, Inborn Errors (D000592) |
Parent Node:
Eye Abnormalities (D005124) |
Parent Node:
Hypercalcemia (D006934) |
Parent Node:
Kidney Diseases (D007674) |
..Starting node
.. Blue diaper syndrome (C536239)
|
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
|
