Familial primary hypomagnesemia with normocalciuria 717788000
SNOMED CT code
| SNOMED code | 717788000 |
|---|---|
| name | Familial primary hypomagnesemia with normocalciuria |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Familial primary hypomagnesemia with normocalciuria (disorder) |
| synonyms |
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| parents | |
| children | Familial primary hypomagnesemia with normocalciuria and normocalcemia 725031005 |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Familial primary hypomagnesemia with normocalciuria 717788000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic disorder of transport 111394006 Primary hypomagnesemia 80710001 Familial primary hypomagnesemia with normocalciuria 717788000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks |
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