Hereditary xanthinuria 54627004
SNOMED CT code
SNOMED code | 54627004 |
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name | Hereditary xanthinuria |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Hereditary xanthinuria (disorder) |
synonyms |
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attributes - group1 | |
Finding site | Kidney structure 64033007 |
parents |
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children | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic renal disease 106000008 Deficiency of xanthine oxidase 124147007 Hereditary xanthinuria 54627004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Hereditary metabolic disease 1821000146108 Hereditary xanthinuria 54627004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of purine and pyrimidine metabolism 238006008 Disorder of purine metabolism 32612005 Hereditary xanthinuria 54627004 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Hereditary nephropathy 367591000119105 Hereditary xanthinuria 54627004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Hereditary xanthinuria 54627004 |
ancestors | sorted most to least specific
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cpt crosswalks |
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