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Terminology chevron_right Concepts chevron_right 80710001

Production

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Component

80710001

The component that hold information about this concept.

Fully Specified Name (FSN)

Primary hypomagnesemia (disorder)

Shortest Term

Primary hypomagnesemia

Definition Status

900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Primary hypomagnesemia (disorder)

SCTID: 80710001, Primitive, Active

80710001|Primary hypomagnesemia (disorder)|

en Primary hypomagnesaemia
en Primary hypomagnesemia
en Primary hypomagnesemia (disorder)

Expression

80710001 |Primary hypomagnesemia (disorder)|
 <<< 111394006 |Metabolic disorder of transport (disorder)| + 
190855004 |Hypomagnesemia (disorder)|

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
504496013 - Primary hypomagnesaemia (en) View
504496013	en	Synonym (core metadata concept)	Primary hypomagnesaemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
133884011 - Primary hypomagnesemia (en) View
133884011	en	Synonym (core metadata concept)	Primary hypomagnesemia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
821900010 - Primary hypomagnesemia (disorder) (en) View
821900010	en	Fully specified name (core metadata concept)	Primary hypomagnesemia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (875550026) - 80710001 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (279200022) - 80710001 -> 111394006 (116680003) View
116680003 \|Is a (attribute)\|	111394006 \|Metabolic disorder of transport (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (279201021) - 80710001 -> 190855004 (116680003) View
116680003 \|Is a (attribute)\|	190855004 \|Hypomagnesemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
111394006 View
111394006	Metabolic disorder of transport (disorder)	Metabolic disorder of transport	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
190855004 View
190855004	Hypomagnesemia (disorder)	Giảm magie máu	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1351854006 View
1351854006	Primary hypomagnesemia, generalized seizures, intellectual disability, obesity syndrome (disorder)	Primary hypomagnesemia, generalized seizures, intellectual disability, obesity syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1351962002 View
1351962002	Epidermal growth factor-related primary hypomagnesemia with intellectual disability (disorder)	Egf-related primary hypomagnesemia with intellectual disability	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1269236003 View
1269236003	Primary hypomagnesemia, refractory seizures, intellectual disability syndrome (disorder)	Primary hypomagnesemia, refractory seizures, intellectual disability syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
725393000 View
725393000	Autosomal dominant primary hypomagnesemia with hypocalciuria (disorder)	Isolated renal magnesium wasting	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
717788000 View
717788000	Familial primary hypomagnesemia with normocalciuria (disorder)	Familial primary hypomagnesemia with normocalciuria	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
721172000 View
721172000	Hypomagnesemia co-occurrent with normocalciuria (disorder)	Hypomagnesemia with normocalciuria	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
722008003 View
722008003	Isolated autosomal dominant hypomagnesemia glaudemans type (disorder)	Isolated autosomal dominant hypomagnesemia glaudemans type	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
711151004 View
711151004	Hypomagnesemia with secondary hypocalcemia (disorder)	Hypomagnesemic tetany	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
707756004 View
707756004	Gitelman syndrome (disorder)	Gitelman syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
24754009 View
24754009	Isolated familial intestinal hypomagnesemia (disorder)	Magnesium malabsorption	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
48655003 View
48655003	Isolated familial renal hypomagnesemia (disorder)	Isolated familial renal hypomagnesemia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
50029007 View
50029007	Familial hypomagnesemia-hypercalciuria (disorder)	Familial hypomagnesemia-hypercalciuria	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (2914d9e1-c800-58d1-b073-6c61ddd53bc4) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E83.4	OTHERWISE TRUE	ALWAYS E83.4	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447637006 \|Map source concept is properly classified (foundation metadata concept)\|
ExtendedMap object (651f7969-89c9-5fb4-93eb-9b78c93bb511) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	OTHERWISE TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|
ExtendedMap object (711d179e-2886-5a4e-936b-c720ea61acc4) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	N15.8	IFA 707755000 \| Familial hypokalemic and hypomagnesemic tubulopathy (disorder) \|	IF FAMILIAL HYPOKALEMIC AND HYPOMAGNESEMIC TUBULOPATHY CHOOSE N15.8 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (7c65734f-25b3-5f62-ba89-b8cf6009de6c) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q87.8	IFA 700448000 \| Epilepsy, ataxia, sensorineural deafness, and tubulopathy syndrome (disorder) \|	IF EPILEPSY, ATAXIA, SENSORINEURAL DEAFNESS, AND TUBULOPATHY SYNDROME CHOOSE Q87.8 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (a6355f1b-974a-57cf-b544-2fb4a854c590) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E83.4	TRUE	ALWAYS E83.4	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447637006 \|Map source concept is properly classified (foundation metadata concept)\|
ExtendedMap object (cf4ea915-0fda-5c64-b7b3-3b3afad09901) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E83.5	IFA 50029007 \| Familial hypomagnesemia-hypercalciuria (disorder) \|	IF FAMILIAL HYPOMAGNESEMIA-HYPERCALCIURIA CHOOSE E83.5 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (2914d9e1-c800-58d1-b073-6c61ddd53bc4) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E83.4	OTHERWISE TRUE	ALWAYS E83.4	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447637006 \|Map source concept is properly classified (foundation metadata concept)\|
ExtendedMap object (651f7969-89c9-5fb4-93eb-9b78c93bb511) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	OTHERWISE TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|
ExtendedMap object (711d179e-2886-5a4e-936b-c720ea61acc4) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	N15.8	IFA 707755000 \| Familial hypokalemic and hypomagnesemic tubulopathy (disorder) \|	IF FAMILIAL HYPOKALEMIC AND HYPOMAGNESEMIC TUBULOPATHY CHOOSE N15.8 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (7c65734f-25b3-5f62-ba89-b8cf6009de6c) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q87.8	IFA 700448000 \| Epilepsy, ataxia, sensorineural deafness, and tubulopathy syndrome (disorder) \|	IF EPILEPSY, ATAXIA, SENSORINEURAL DEAFNESS, AND TUBULOPATHY SYNDROME CHOOSE Q87.8 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (a6355f1b-974a-57cf-b544-2fb4a854c590) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E83.4	TRUE	ALWAYS E83.4	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447637006 \|Map source concept is properly classified (foundation metadata concept)\|
ExtendedMap object (cf4ea915-0fda-5c64-b7b3-3b3afad09901) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E83.5	IFA 50029007 \| Familial hypomagnesemia-hypercalciuria (disorder) \|	IF FAMILIAL HYPOMAGNESEMIA-HYPERCALCIURIA CHOOSE E83.5 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|

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