Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement 725033008
SNOMED CT code
SNOMED code | 725033008 |
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name | Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement |
status | active |
date introduced | 2017-07-31 |
fully specified name(s) | Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (disorder) |
synonyms |
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attributes - group1 | |
Finding site | Structure of parenchyma of kidney 29704000 |
Associated morphology | Pathologic calcification 18115005 |
parents |
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hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Hereditary nephropathy 367591000119105 Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement 725033008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic renal disease 106000008 Nephrocalcinosis 48638002 Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement 725033008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic disorder of transport 111394006 Primary hypomagnesemia 80710001 Familial hypomagnesemia-hypercalciuria 50029007 Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement 725033008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement 725033008 |
ancestors | sorted most to least specific
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cpt crosswalks |
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