Mucopolysaccharidosis-like plus disease 1187113001
SNOMED CT code
| SNOMED code | 1187113001 |
|---|---|
| name | Mucopolysaccharidosis-like plus disease |
| status | active |
| date introduced | 2021-11-30 |
| fully specified name(s) | Mucopolysaccharidosis-like plus disease (disorder) |
| synonyms |
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| attributes - group4 | |
| Finding site | Respiratory system structure 20139000 |
| attributes - group5 | |
| Finding site | Hematopoietic system structure 57171008 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Bone structure 272673000 |
| Associated morphology | Dysplasia 25723000 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Heart structure 80891009 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| Finding site | Face structure 89545001 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Cardiovascular finding 106063007 Cardiac finding 301095005 Heart disease 56265001 Structural disorder of heart 128599005 Congenital heart disease 13213009 Mucopolysaccharidosis-like plus disease 1187113001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental delay 248290002 Global developmental delay 224958001 Mucopolysaccharidosis-like plus disease 1187113001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Disorder of lysosomal enzyme 23585005 Dysostosis multiplex group 279081001 Mucopolysaccharidosis-like plus disease 1187113001 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Disorder of cardiovascular system 49601007 Cardiovascular system hereditary disorder 363005004 Mucopolysaccharidosis-like plus disease 1187113001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Mucopolysaccharidosis-like plus disease 1187113001 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Mucopolysaccharidosis-like plus disease 1187113001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of hematopoietic structure 414027002 Mucopolysaccharidosis-like plus disease 1187113001 SNOMED CT Concept 138875005 Clinical finding 404684003 Respiratory finding 106048009 Disorder of respiratory system 50043002 Mucopolysaccharidosis-like plus disease 1187113001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disorder of face 118930001 Congenital anomaly of face 398302004 Multiple malformation syndrome with facial defects as major feature 65094009 Mucopolysaccharidosis-like plus disease 1187113001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Mucopolysaccharidosis-like plus disease 1187113001 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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