Concept information
Preferred term
Metabolic renal disease
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Narrower concepts
- Bartter syndrome (disorder)
- Cholemic nephrosis
- Cystinuria
- Deficiency of hypoxanthine oxidase
- Dysmorphic sialidosis with renal involvement
- Fabry's disease
- Familial arthrogryposis-cholestatic hepatorenal syndrome
- Familial hypokalemic alkalosis, Gullner type
- Familial methionine malabsorption
- Fanconi syndrome
- Glycogenosis with glucoaminophosphaturia
- Histidine transport defect
- Hypercalcemic nephropathy
- Hyperkalemia, diminished renal excretion
- Hypokalemic nephropathy
- Hypoxic nephrosis
- Iminoglycinuria
- Isolated familial renal hypomagnesemia
- Lowe syndrome
- Milk alkali syndrome
- Neutral 1 amino acid transport defect
- Primary hyperoxaluria
- Renal hemosiderosis
- Renal medullary washout (disorder)
- Renal phosphaturia
- Salt-wasting syndrome of infancy
- Secondary oxalosis
- Volume excess, primary renal sodium retention
Finding site
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/106000008
{{label}}
{{#each values }} {{! loop through ConceptPropertyValue objects }}
{{#if prefLabel }}
{{/if}}
{{/each}}
{{#if notation }}{{ notation }} {{/if}}{{ prefLabel }}
{{#ifDifferentLabelLang lang }} ({{ lang }}){{/ifDifferentLabelLang}}
{{#if vocabName }}
{{ vocabName }}
{{/if}}