Congenital nephrotic syndrome with focal glomerulosclerosis 236384008
SNOMED CT code
| SNOMED code | 236384008 |
|---|---|
| name | Congenital nephrotic syndrome with focal glomerulosclerosis |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Congenital nephrotic syndrome with focal glomerulosclerosis (disorder) |
| synonyms | Congenital nephrotic syndrome with focal glomerulosclerosis |
| attributes - group1 | |
| Interprets | Albumin measurement 26758005 |
| Has interpretation | Below reference range 281300000 |
| attributes - group2 | |
| Interprets | Urine protein measurement 57378007 |
| Has interpretation | Above reference range 281302008 |
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Glomerulosclerosis 82646005 |
| Finding site | Glomerulus structure 68288006 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Glomerulosclerosis 197661001 Congenital nephrotic syndrome with focal glomerulosclerosis 236384008 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Hereditary nephropathy 367591000119105 Congenital nephrotic syndrome with focal glomerulosclerosis 236384008 SNOMED CT Concept 138875005 Clinical 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 Congenital nephrotic syndrome with focal glomerulosclerosis 236384008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital nephrotic syndrome with focal glomerulosclerosis 236384008 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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