Hypomagnesemia with secondary hypocalcemia 711151004
SNOMED CT code
| SNOMED code | 711151004 |
|---|---|
| name | Hypomagnesemia with secondary hypocalcemia |
| status | active |
| date introduced | 2015-07-31 |
| fully specified name(s) | Hypomagnesemia with secondary hypocalcemia (disorder) |
| synonyms |
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| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Nervous system structure 25087005 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Parathyroid structure 111002 |
| attributes - group3 | |
| Interprets | Hormone secretion 60877009 |
| Has interpretation | Decreased 1250004 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Endocrine finding 106176003 Decreased hormone secretion 42497006 Hypoparathyroidism 36976004 Parathyroid hypocalcemic tetany 16195001 Hypomagnesemia with secondary hypocalcemia 711151004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 Hypomagnesemia with secondary hypocalcemia 711151004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Hypomagnesemia with secondary hypocalcemia 711151004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Hypomagnesemia with secondary hypocalcemia 711151004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic disorder of transport 111394006 Primary hypomagnesemia 80710001 Hypomagnesemia with secondary hypocalcemia 711151004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Hypomagnesemia with secondary hypocalcemia 711151004 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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