Autosomal recessive hypophosphatemic bone disease 237891005
SNOMED CT code
| SNOMED code | 237891005 |
|---|---|
| name | Autosomal recessive hypophosphatemic bone disease |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Autosomal recessive hypophosphatemic bone disease (disorder) |
| synonyms |
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| attributes - group1 | |
| Finding site | Osteoid tissue 39365008 |
| parents | |
| children | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of mineral metabolism 45744005 Disorder with defective osteoid mineralization 126533001 Autosomal recessive hypophosphatemic bone disease 237891005 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Autosomal recessive hypophosphatemic bone disease 237891005 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 recessive hypophosphatemic bone disease 237891005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Autosomal recessive hypophosphatemic bone disease 237891005 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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