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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
CAKUT +     
kidney disease +     
46,XX Sex Reversal with Dysgenesis of Kidneys, Adrenals, and Lungs  
AIDS-Associated Nephropathy  
Alsing Syndrome 
anuria +   
apolipoprotein A-IV associated amyloidosis 
Arnold Stickler Bourne Syndrome 
atheroembolism of kidney 
autoimmune interstitial lung, joint, and kidney disease  
Bifid Nose with or without Anorectal and Renal Anomalies  
BILIARY, RENAL, NEUROLOGIC, AND SKELETAL SYNDROME  
BLADDER DYSFUNCTION, AUTONOMIC, WITH IMPAIRED PUPILLARY REFLEX AND SECONDARY CAKUT  
Blue Diaper Syndrome 
CAKUT1  
A CAKUT that has_material_basis_in heterozygous mutation in the DSTYK gene on chromosome 1q32. (DO)
CAKUT2  
CAKUT3  
Complement Factor H Deficiency  
cystic kidney disease +   
diabetes insipidus +   
Diabetic Nephropathies  
dialysis-related amyloidosis 
Dimauro Disease  
dioctophymiasis 
Epidermolysis Bullosa Simplex 7, with Nephropathy and Deafness  
familial juvenile hyperuricemic nephropathy +   
Glomerular Diseases +   
Goodpasture syndrome +   
granulomatosis with polyangiitis +   
Hantavirus hemorrhagic fever with renal syndrome +   
Herrmann Syndrome 
Hydranencephaly with Renal Aplasia-Dysplasia  
hydronephrosis +   
Hyperoxaluria +   
hypophosphatemic nephrolithiasis/osteoporosis +   
Ichthyosis, Mental Retardation, Dwarfism, and Renal Impairment 
immunoglobulin heavy chain amyloidosis 
immunoglobulin light chain amyloidosis  
Infundibulopelvic Dysgenesis 
Jejunal Atresia with Renal Adysplasia 
Joubert syndrome 5  
Joubert syndrome 6  
Joubert syndrome 9  
kidney cortex disease +   
kidney failure +   
kidney hypertrophy 
Kidney Neoplasms +   
kidney papillary necrosis 
Lachiewicz Sibley Syndrome 
Lipoprotein Glomerulopathy  
Lymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus  
nephritis +   
nephrocalcinosis +   
nephrogenic diabetes insipidus +   
nephrolithiasis +   
nephrosclerosis +   
nephrotoxicity  
neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities  
NEURODEVELOPMENTAL-CRANIOFACIAL SYNDROME WITH VARIABLE RENAL AND CARDIAC ABNORMALITIES  
NEUROOCULORENAL SYNDROME  
obstructive nephropathy  
orthostatic proteinuria 
perinephritis 
Premature Atherosclerosis with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease 
proteinuria +   
pyelitis +   
Radiation Nephropathy  
Radio Renal Syndrome 
renal agenesis +   
renal artery disease +   
renal artery obstruction +   
renal coloboma syndrome  
Renal Dysplasia - Limb Defects Syndrome 
renal fibrosis +   
renal hypertension +   
renal hypoplasia +   
renal infectious disease 
Renal Ischemia  
Renal Nutcracker Syndrome 
renal osteodystrophy  
renal tuberculosis  
Renal Tubular Dysgenesis +   
renal tubular transport disease +   
Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia due to Duplication of Mitochondrial DNA 
secondary hyperparathyroidism of renal origin 
Selig Benacerraf Greene Syndrome 
serum amyloid A amyloidosis 
Siegler Brewer Carey Syndrome 
Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, and Progressive Nephropathy 
stricture or kinking of ureter 
Thrombocytopenia with Elevated Serum Iga and Renal Disease 
Thyrocerebral-Retinal Syndrome 
uremia +   
Webb-Dattani Syndrome  
Zellweger syndrome +   

Synonyms
Exact Synonyms: RHDNS1 ;   congenital anomalies of kidney and urinary tract 1 ;   congenital anomalies of the kidney and urinary tract 1 ;   nonsyndromic renal hypodysplasia 1
Related Synonyms: CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 1, SUSCEPTIBILITY TO
Primary IDs: MESH:C563661
Alternate IDs: OMIM:610805
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/23862974 "DO" "DO"

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