Mannosidosis 65524005
SNOMED CT code
| SNOMED code | 65524005 |
|---|---|
| name | Mannosidosis |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Mannosidosis (disorder) |
| synonyms |
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| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Dysplasia 25723000 |
| 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 Oligosaccharidosis 1155842003 Mannosidosis 65524005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Disorder of lysosomal enzyme 23585005 Dysostosis multiplex group 279081001 Mannosidosis 65524005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Mannosidosis 65524005 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Mannosidosis 65524005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Mannosidosis 65524005 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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