Metabolic renal disease (disorder)
| Code | 106000008 |
|---|---|
| Semantic tag | disorder |
| Module | international |
| Definition | defined |
| Effective time | 20220228 |
90708001Kidney disease
disorder
75934005Metabolic disease
disorder
720519003Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome
disorder
707742001Bartter syndrome
disorder
42927005Cholaemic nephrosis
disorder
78544004Chronic hypertensive uraemia
disorder
1388279003Chronic tubulointerstitial nephritis caused by lead with hyperuricaemia
disorder
85020001Cystinuria
disorder
124147007Deficiency of xanthine oxidase
disorder
236475007Dibasic aminoaciduria
disorder
783620009Dominant hypophosphataemia with nephrolithiasis and/or osteoporosis
disorder
81896006Dysmorphic sialidosis with renal involvement
disorder
1351962002EGF-related primary hypomagnesaemia with intellectual disability
disorder
763280005Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome
disorder
16652001Fabry's disease
disorder
62216007Familial arthrogryposis-cholestatic hepatorenal syndrome
disorder
81987005Familial hypokalaemic alkalosis, Gullner type
disorder
45812003Familial methionine malabsorption
disorder
1187040004Familial steroid-resistant nephrotic syndrome with adrenal insufficiency
disorder
40488004Fanconi syndrome
disorder
1363284002Gitelman-like kidney tubulopathy due to mitochondrial DNA mutation
disorder
236477004Glycinuria
disorder
61598006Glycogenosis with glucoaminophosphaturia
disorder
1217380005HELIX syndrome
disorder
78311009Histidine transport defect
disorder
33763006Hypercalcaemic nephropathy
disorder
54781007Hyperkalaemia, diminished renal excretion
disorder
367621000119107Hyperoxaluria
disorder
776416004Hyperuricaemia, pulmonary hypertension, renal failure, alkalosis syndrome
disorder
54879000Hypokalaemic nephropathy
disorder
67132008Hypoxic nephrosis
disorder
84121007Iminoglycinuria
disorder
62332007Infantile nephropathic cystinosis
disorder
48655003Isolated familial renal hypomagnesaemia
disorder
722457005Juvenile cataract, microcornea, renal glucosuria syndrome
disorder
95582003Kidney crystallisation
disorder
446923008Lipoprotein glomerulopathy
disorder
79385002Lowe syndrome
disorder
43258006Milk alkali syndrome
disorder
782771007Mitochondrial DNA depletion syndrome hepatocerebrorenal form
disorder
48638002Nephrocalcinosis
disorder
80902009Neutral 1 amino acid transport defect
disorder
237612000Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction
disorder
1351854006Primary hypomagnesaemia, generalised seizures, intellectual disability, obesity syndrome
disorder
21764004Renal carnitine transport defect
disorder
83563007Renal haemosiderosis
disorder
735475005Renal hypocalciuria
disorder
370493008Renal medullary washout
disorder
85487008Renal phosphaturia
disorder
81986001Renal secondary osteodystrophia fibrosa
disorder
1776003Renal tubular acidosis
disorder
717053007Renal tubulopathy with encephalopathy and liver failure syndrome
disorder
53378008Salt-wasting syndrome of infancy
disorder
41305006Secondary oxalosis
disorder
717263009Transient pseudohypoaldosteronism
disorder
236495001Urate nephropathy
disorder