Autosomal dominant hypophosphatemic rickets 237889002
SNOMED CT code
| SNOMED code | 237889002 |
|---|---|
| name | Autosomal dominant hypophosphatemic rickets |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Autosomal dominant hypophosphatemic rickets (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Osteoid tissue 39365008 |
| Associated morphology | Dysplasia 25723000 |
| attributes - group2 | |
| Associated morphology | Impaired mineralization 128416000 |
| Finding site | Bone structure 272673000 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| attributes - group3 | |
| Due to | Specific renal tubule transport defect 236470002 |
| attributes - group5 | |
| Finding site | Structure of epiphyseal plate 711190000 |
| attributes - group4 | |
| Interprets | Physiologic mineralization of bone 128417009 |
| Has interpretation | Deficient 260372006 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic bone disease 50279003 Autosomal dominant hypophosphatemic bone disease 237890006 Autosomal dominant hypophosphatemic rickets 237889002 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Joint finding 118952005 Arthropathy 399269003 Arthropathy associated with another disorder 35524003 Autosomal dominant hypophosphatemic rickets 237889002 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Rickets 41345002 Autosomal dominant hypophosphatemic rickets 237889002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
Thank you for choosing Find-A-Code, please Sign In to remove ads.
Quick, Current, Complete - www.findacode.com