Morquio syndrome 378007
SNOMED CT code
SNOMED code | 378007 |
---|---|
name | Morquio syndrome |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Morquio syndrome (disorder) |
synonyms |
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attributes - group1 | |
Occurrence | Congenital 255399007 |
Associated morphology | Dystrophy 4720007 |
Finding site | Bone structure 272673000 |
parents |
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children | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Disorder of lysosomal enzyme 23585005 Mucopolysaccharidosis 11380006 Morquio syndrome 378007 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Morquio syndrome 378007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic bone disease 50279003 Morquio syndrome 378007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital osteodystrophy 5731000119108 Morquio syndrome 378007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Morquio syndrome 378007 |
ancestors | sorted most to least specific
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cpt crosswalks |
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