Galloway Mowat syndrome 721297008
SNOMED CT code
| SNOMED code | 721297008 |
|---|---|
| name | Galloway Mowat syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Galloway Mowat syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Finding site | Central nervous system structure 21483005 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Glomerulus structure 68288006 |
| attributes - group4 | |
| Interprets | Albumin measurement 26758005 |
| Has interpretation | Below reference range 281300000 |
| attributes - group3 | |
| Interprets | Urine protein measurement 57378007 |
| Has interpretation | Above reference range 281302008 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Urine finding 301830001 Finding of urine substance level 785672002 Urine substance level above reference range 1217345006 Proteinuria 29738008 Protein-losing nephropathy 370494002 Nephrotic syndrome 52254009 Steroid-resistant nephrotic syndrome 236381000 Galloway Mowat syndrome 721297008 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 Congenital anomaly of central nervous system 128124001 Disorder of neuronal migration and differentiation 253146009 Galloway Mowat syndrome 721297008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Galloway Mowat syndrome 721297008 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 Galloway Mowat syndrome 721297008 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Hereditary nephropathy 367591000119105 Galloway Mowat syndrome 721297008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Galloway Mowat syndrome 721297008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Galloway Mowat syndrome 721297008 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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