Familial arthrogryposis-cholestatic hepatorenal syndrome 62216007
SNOMED CT code
| SNOMED code | 62216007 |
|---|---|
| name | Familial arthrogryposis-cholestatic hepatorenal syndrome |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Familial arthrogryposis-cholestatic hepatorenal syndrome (disorder) |
| synonyms |
|
| attributes - group2 | |
| Has interpretation | Decreased 1250004 |
| Interprets | Range of joint movement 364564000 |
| attributes - group4 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Structure of joint region 785818007 |
| Associated morphology | Contracture 57048009 |
| Occurrence | Congenital 255399007 |
| attributes - group7 | |
| Interprets | Renal function 11953005 |
| Has interpretation | Impaired 260379002 |
| attributes - group3 | |
| Finding site | Kidney structure 64033007 |
| attributes - group6 | |
| Finding site | Liver structure 10200004 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic renal disease 106000008 Familial arthrogryposis-cholestatic hepatorenal syndrome 62216007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Familial disease 111941005 Familial arthrogryposis-cholestatic hepatorenal syndrome 62216007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Inherited arthrogryposis 28204005 Familial arthrogryposis-cholestatic hepatorenal syndrome 62216007 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Familial arthrogryposis-cholestatic hepatorenal syndrome 62216007 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Hereditary nephropathy 367591000119105 Familial arthrogryposis-cholestatic hepatorenal syndrome 62216007 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Finding of renal function 1148582006 Renal impairment 236423003 Renal failure syndrome 42399005 Hepatorenal syndrome 51292008 Familial arthrogryposis-cholestatic hepatorenal syndrome 62216007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Inherited disorder of bilirubin metabolism 5655007 Familial arthrogryposis-cholestatic hepatorenal syndrome 62216007 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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