Metabolic renal disease 106000008 SNOMED CT code SNOMED code 106000008 name Metabolic renal disease status active date introduced 2002-01-31 fully specified name(s) Metabolic renal disease (disorder) synonyms Metabolic disorders of the kidney Metabolic renal disease attributes - group1 Finding site Kidney structure 64033007 parents children Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome 720519003 Bartter syndrome 707742001 Cholemic nephrosis 42927005 Cystinuria 85020001 Deficiency of xanthine oxidase 124147007 Dibasic aminoaciduria 236475007 Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis 783620009 Dysmorphic sialidosis with renal involvement 81896006 Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome 763280005 Fabry's disease 16652001 Familial arthrogryposis-cholestatic hepatorenal syndrome 62216007 Familial hypokalemic alkalosis, Gullner type 81987005 Familial methionine malabsorption 45812003 Familial steroid-resistant nephrotic syndrome with adrenal insufficiency 1187040004 Fanconi syndrome 40488004 Glycinuria 236477004 Glycogenosis with glucoaminophosphaturia 61598006 HELIX syndrome 1217380005 Histidine transport defect 78311009 Hypercalcemic nephropathy 33763006 Hyperkalemia, diminished renal excretion 54781007 Hyperoxaluria 367621000119107 Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome 776416004 Hypokalemic nephropathy 54879000 Hypoxic nephrosis 67132008 Iminoglycinuria 84121007 Infantile nephropathic cystinosis 62332007 Isolated familial renal hypomagnesemia 48655003 Juvenile cataract, microcornea, renal glucosuria syndrome 722457005 Kidney crystallization 95582003 Leigh syndrome with nephrotic syndrome 783157004 Lipoprotein glomerulopathy 446923008 Lowe syndrome 79385002 Milk alkali syndrome 43258006 Mitochondrial DNA depletion syndrome hepatocerebrorenal form 782771007 Nephrocalcinosis 48638002 Nephrogenic diabetes insipidus 111395007 Neutral 1 amino acid transport defect 80902009 Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction 237612000 Primary hyperoxaluria 17901006 Renal carnitine transport defect 21764004 Renal hemosiderosis 83563007 Renal hypocalciuria 735475005 Renal medullary washout 370493008 Renal phosphaturia 85487008 Renal secondary osteodystrophia fibrosa 81986001 Renal tubular acidosis 1776003 Salt-wasting syndrome of infancy 53378008 Secondary oxalosis 41305006 Transient pseudohypoaldosteronism 717263009 Urate nephropathy 236495001 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 64572001 75934005 106000008 138875005 404684003 406123005 249561001 249578005 90708001 106000008 ancestors sorted most to least specific
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