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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
metabolic disease +     
acquired metabolic disease +   
ALG13-CDG 
amino acid metabolism disease +   
amino-acid transport disorder 
Autism spectrum disorder-epilepsy-arthrogryposis syndrome 
Autosomal dominant primary hypomagnesemia with hypocalciuria 
Autosomal recessive limb-girdle muscular dystrophy due to ISPD deficiency 
bilirubin metabolism disease +   
carbohydrate metabolism disease +   
chondrocalcinosis +  
chronic pyelonephritis +  
chronic rapidly progressive glomerulonephritis 
chronic renal failure syndrome 
CHST3-related skeletal dysplasia 
Chédiak-Higashi syndrome 
Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome 
Congenital atransferrinemia 
congenital chronic kidney disease 
Congenital dyserythropoietic anemia type II 
Congenital muscular dystrophy, Fukuyama type 
developmental anomaly of metabolic origin +  
diabetic nephropathy +   
Diabetic nephropathy (sometimes called Kimmelstiel-Wilson syndrome) is a progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis. Progressive kidney disorder caused by vascular damage to the glomerular capillaries, in patients with diabetes mellitus. It is usually manifested with nephritic syndrome and glomerulosclerosis.
diabetic retinopathy +   
disorder of acid-base balance +   
Disorder of amino acid and other organic acid metabolism +  
Disorder of biogenic amine metabolism and transport +  
Disorder of carbohydrate metabolism +  
Disorder of energy metabolism +  
Disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation +  
disorder of glycosylation +  
Disorder of lipid metabolism +   
disorder of organic acid metabolism +  
Disorder of porphyrin and haem metabolism +  
Disorder of purine or pyrimidine metabolism +   
Disorder of vitamin and non-protein cofactor absorption and transport  +  
Distal myopathy, Nonaka type 
dopa-responsive dystonia +  
DPM1-CDG 
Ehlers-Danlos syndrome, progeroid type 
FTH1-related iron overload 
glucose metabolism disease +   
glutaric aciduria +  
gout +   
hemochromatosis 
hepatic methionine adenosyltransferase deficiency 
hyperamylasemia 
hyperlipidemia +   
hyperlipoproteinemia +   
hyperprolactinemia +  
Hypertriglyceridemia +   
hypoalphalipoproteinemia +  
inborn errors of metabolism +   
lactic acidosis +  
lipodystrophy +  
Lysosomal disease +  
metabolic syndrome  
metabolic toxicity 
methylmalonic aciduria (cobalamin deficiency) cblA type 
mineral metabolism disease +   
muscular dystrophy, congenital, with cataracts and intellectual disability 
nutritional disorder +   
Other metabolic disease +  
Papillon-Lefèvre syndrome 
Peroxisomal beta-oxidation disorder +  
peroxisome biogenesis disorder, complementation group 7 
Peroxisome biogenesis disorder-Zellweger syndrome spectrum +  
porphyrin metabolism disease +  
Primary hypomagnesemia with secondary hypocalcemia 
proteostasis deficiencies +   
purine metabolism disease +  
pyrimidine metabolism disease +  
Rare hereditary hemochromatosis 
Recurrent infections - inflammatory syndrome due to zinc metabolism disorder 
Refsum disease 
stage 5 chronic kidney disease  
steroid dehydrogenase deficiency-dental anomalies syndrome 
steroid metabolism disease +  
Tumor Lysis Syndrome 
x-linked warfarin sensitivity 
xanthinuria +  
xanthoma 

Synonyms
Exact Synonyms: DKD ;   DMII RENAL UNCNTRLD ;   DMII RENL NT ST UNCNTRLD ;   Diabetes with renal manifestations ;   Diabetes with renal manifestations (disorder) ;   Diabetes-nephrosis syndrome ;   Diabetes-nephrosis syndrome (disorder) ;   Diabetic Glomerulosclerosis ;   Diabetic Kidney Disease ;   Diabetic Kidney Diseases
Narrow Synonyms: type 1 diabetes nephropathy ;   type 2 diabetes nephropathy
Xrefs: DOID:9002165 ;   ICD9:250.4 ;   ICD9:250.40 ;   ICD9:583.81 ;   MEDGEN:8352 ;   MESH:D003928 ;   MIM:612624 ;   MIM:612628 ;   MIM:612634 ;   MONDO:0005016
External Ontologys: disease_arises_from_feature disease_arises_from_feature EFO:0000400 ;   has_disease_location EFO:UBERON:0002113
Definition Sources: NCIT:C84417

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