Primary hyperoxaluria 17901006
SNOMED CT code
| SNOMED code | 17901006 | ||
|---|---|---|---|
| name | Primary hyperoxaluria | ||
| status | active | ||
| date introduced | 2002-01-31 | ||
| fully specified name(s) | Primary hyperoxaluria (disorder) | ||
| synonyms |
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| attributes - group2 | |||
| Finding site | Kidney structure 64033007 | ||
| attributes - group1 | |||
| Occurrence | Congenital 255399007 | ||
| parents | |||
| children | |||
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic renal disease 106000008 Primary hyperoxaluria 17901006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of carbohydrate metabolism 20957000 Primary hyperoxaluria 17901006 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Hereditary nephropathy 367591000119105 Primary hyperoxaluria 17901006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Enzymopathy 78548001 Primary hyperoxaluria 17901006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Primary hyperoxaluria 17901006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Primary hyperoxaluria 17901006 | ||
| ancestors | sorted most to least specific
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| cpt crosswalks |
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