Thyrocerebrorenal syndrome 733096007
SNOMED CT code
| SNOMED code | 733096007 |
|---|---|
| name | Thyrocerebrorenal syndrome |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Thyrocerebrorenal syndrome (disorder) |
| synonyms |
|
| attributes - group2 | |
| Interprets | Hemostatic function 74848003 |
| Has interpretation | Abnormal 263654008 |
| attributes - group4 | |
| Occurrence | Congenital 255399007 |
| Finding site | Cerebrum 83678007 |
| attributes - group5 | |
| Occurrence | Congenital 255399007 |
| Finding site | Thyroid structure 69748006 |
| attributes - group6 | |
| Has interpretation | Below reference range 281300000 |
| Interprets | Platelet count 61928009 |
| attributes - group7 | |
| Occurrence | Congenital 255399007 |
| Finding site | Kidney structure 64033007 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of neck 118939000 Disorder of thyroid gland 14304000 Thyrocerebrorenal syndrome 733096007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 Thyrocerebrorenal syndrome 733096007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Thyrocerebrorenal syndrome 733096007 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Hereditary nephropathy 367591000119105 Thyrocerebrorenal syndrome 733096007 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Disorder of hemostatic system 362970003 Platelet disorder 22716005 Inherited platelet disorder 234469001 Hereditary thrombocytopenic disorder 438492008 Thyrocerebrorenal syndrome 733096007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital thrombocytopenia 737221003 Thyrocerebrorenal syndrome 733096007 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Disorder of brain 81308009 Thyrocerebrorenal syndrome 733096007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Thyrocerebrorenal syndrome 733096007 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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