OMOP Concept 4024556
Metabolic renal disease
StandardConditionSNOMED106000008Disorder
Maps from
1
Descendants
112
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Metabolic renal disease via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 106000008 | Metabolic disorders of the kidney | Non-standard |
Synonyms
Alternative names recorded for Metabolic renal disease across source vocabularies.
- Metabolic disorders of the kidney
- Metabolic renal disease (disorder)
- nefropatía metabólica
- nefropatía metabólica (trastorno)
- trastorno metabólico del riñón
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(20)Roll up to these when you need a wider cohort.
- 1Kidney disease
- 1Metabolic disease
- 2Disease
- 2Disorder of kidney and/or ureter
- 2Disorder of retroperitoneum
- 2Kidney finding
- 3Abdominal organ finding
- 3Clinical finding
- 3Disorder of abdomen
- 3Disorder of urinary system
- 3Urinary system finding
- 4Disorder of abdominopelvic segment of trunk
- 4Disorder of the genitourinary system
- 4Finding of abdomen
- 4Urogenital finding
- 4Viscus structure finding
- 5Disorder of body system
- 5Disorder of trunk
- 5Finding of abdominopelvic segment of trunk
- 6Finding of trunk structure
Narrower concepts
(112)Included automatically when you query with descendants.
- 1Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome
- 1Bartter syndrome
- 1Cholemic nephrosis
- 1Cystinuria
- 1Deficiency of xanthine oxidase
- 1Dibasic aminoaciduria
- 1Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis
- 1Dysmorphic sialidosis with renal involvement
- 1EGF-related primary hypomagnesemia with intellectual disability
- 1Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome
- 1Fabry's disease
- 1Familial arthrogryposis-cholestatic hepatorenal syndrome
- 1Familial hypokalemic alkalosis, Gullner type
- 1Familial methionine malabsorption
- 1Familial steroid-resistant nephrotic syndrome with adrenal insufficiency
- 1Fanconi syndrome
- 1Glycinuria
- 1Glycogenosis with glucoaminophosphaturia
- 1HELIX syndrome
- 1Histidine transport defect
- 1Hypercalcemic nephropathy
- 1Hyperkalemia, diminished renal excretion
- 1Hyperoxaluria
- 1Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome
- 1Hypokalemic nephropathy
- 1Hypoxic nephrosis
- 1Iminoglycinuria
- 1Infantile nephropathic cystinosis
- 1Isolated familial renal hypomagnesemia
- 1Juvenile cataract, microcornea, renal glucosuria syndrome
- 1Kidney crystallization
- 1Lipoprotein glomerulopathy
- 1Lowe syndrome
- 1Milk alkali syndrome
- 1Mitochondrial DNA depletion syndrome hepatocerebrorenal form
- 1Nephrocalcinosis
- 1Neutral 1 amino acid transport defect
- 1Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction
- 1Primary hyperoxaluria
- 1Primary hypomagnesemia, generalized seizures, intellectual disability, obesity syndrome
- 1Renal carnitine transport defect
- 1Renal hemosiderosis
- 1Renal hypocalciuria
- 1Renal medullary washout
- 1Renal phosphaturia
- 1Renal secondary osteodystrophia fibrosa
- 1Renal tubular acidosis
- 1Salt-wasting syndrome of infancy
- 1Secondary oxalosis
- 1Transient pseudohypoaldosteronism
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