Familial renal iminoglycinuria 75652008
SNOMED CT code
SNOMED code | 75652008 |
---|---|
name | Familial renal iminoglycinuria |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Familial renal iminoglycinuria (disorder) |
synonyms | Familial renal iminoglycinuria |
attributes - group2 | |
Finding site | Kidney structure 64033007 |
attributes - group1 | |
Occurrence | Congenital 255399007 |
parents |
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hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Familial disease 111941005 Familial renal iminoglycinuria 75652008 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Hereditary nephropathy 367591000119105 Familial renal iminoglycinuria 75652008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic renal disease 106000008 Iminoglycinuria 84121007 Familial renal iminoglycinuria 75652008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Familial renal iminoglycinuria 75652008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Familial renal iminoglycinuria 75652008 |
ancestors | sorted most to least specific
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cpt crosswalks |
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