Autosomal dominant primary hypomagnesemia with hypocalciuria 725393000
SNOMED CT code
| SNOMED code | 725393000 |
|---|---|
| name | Autosomal dominant primary hypomagnesemia with hypocalciuria |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Autosomal dominant primary hypomagnesemia with hypocalciuria (disorder) |
| synonyms |
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| parents | |
| 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 primary hypomagnesemia with hypocalciuria 725393000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic disorder of transport 111394006 Primary hypomagnesemia 80710001 Autosomal dominant primary hypomagnesemia with hypocalciuria 725393000 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 calcium metabolism 71638002 Hypocalciuria 86353007 Autosomal dominant primary hypomagnesemia with hypocalciuria 725393000 |
| ancestors | sorted most to least specific
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| cpt crosswalks |
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