Adult hypophosphatasia 20756002
SNOMED CT code
SNOMED code | 20756002 |
---|---|
name | Adult hypophosphatasia |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Adult hypophosphatasia (disorder) |
synonyms |
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attributes - group2 | |
Occurrence | Congenital 255399007 |
attributes - group1 | |
Occurrence | Adulthood 41847000 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Adult hypophosphatasia 20756002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Hypophosphatasia 190859005 Adult hypophosphatasia 20756002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Enzymopathy 78548001 Adult hypophosphatasia 20756002 |
ancestors | sorted most to least specific
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cpt crosswalks |
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