Autosomal dominant hypophosphatemic bone disease 237890006
SNOMED CT code
| SNOMED code | 237890006 |
|---|---|
| name | Autosomal dominant hypophosphatemic bone disease |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Autosomal dominant hypophosphatemic bone disease (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 |
| parents | |
| children | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Autosomal dominant hypophosphatemic bone disease 237890006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of bone development 371521007 Congenital anomaly of skeletal bone 8447006 Dysplasia with defective mineralization 254117007 Autosomal dominant hypophosphatemic bone disease 237890006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Autosomal dominant hypophosphatemic bone disease 237890006 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Autosomal dominant hypophosphatemic bone disease 237890006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of mineral metabolism 45744005 Disorder of phosphate, calcium and vitamin D metabolism 237879001 Disorder of phosphorus metabolism 87049008 Hypophosphatemia 4996001 Autosomal dominant hypophosphatemic bone disease 237890006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic bone disease 50279003 Autosomal dominant hypophosphatemic bone disease 237890006 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Bone finding 118953000 Disorder of bone 76069003 Lesion of bone 879976004 Autosomal dominant hypophosphatemic bone disease 237890006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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