Cystinuria, type 1 37183000
SNOMED CT code
| SNOMED code | 37183000 |
|---|---|
| name | Cystinuria, type 1 |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Cystinuria, type 1 (disorder) |
| synonyms |
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| attributes - group1 | |
| Finding site | Skeletal muscle structure 127954009 |
| attributes - group3 | |
| Interprets | Muscle tone 6918002 |
| attributes - group2 | |
| Finding site | Kidney structure 64033007 |
| parents | |
| children | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Cystinuria, type 1 37183000 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Hereditary nephropathy 367591000119105 Cystinuria, type 1 37183000 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Poor muscle tone 398152000 Cystinuria, type 1 37183000 SNOMED CT Concept 138875005 Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Disorder of skeletal muscle 75047002 Cystinuria, type 1 37183000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic renal disease 106000008 Cystinuria 85020001 Cystinuria, type 1 37183000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Cystinuria, type 1 37183000 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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