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Terminology chevron_right Concepts chevron_right 725033008

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725033008
The component that hold information about this concept.
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (disorder)
Renal hypomagnesemia type 3
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

Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (disorder)

SCTID: 725033008, Primitive, Active


725033008|Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (disorder)|
  • vi Giảm magne huyết nguyên phát gia đình với tăng calci niệu và nhiễm calci thận mà không có liên quan đến mắt nặng
  • en Familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis without severe ocular involvement
  • en Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement
  • en Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (disorder)
  • en Renal hypomagnesaemia type 3
  • en Renal hypomagnesemia type 3

725033008 |Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (disorder)|

<<< 1304111007 |Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 18115005 |Pathologic calcification, calcified structure (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 29704000 |Structure of parenchyma of kidney (body structure)| }
        { 363713009 |Has interpretation (attribute)| = 281302008 |Above reference range (qualifier value)|,
          363714003 |Interprets (attribute)| = 73668004 |Calcium measurement, urine (procedure)| }
Active

7791000269118 - giảm magne huyết nguyên phát gia đình với tăng calci niệu và nhiễm calci thận mà không có liên quan đến mắt nặng (vi) View

7791000269118
vi
Synonym (core metadata concept)
giảm magne huyết nguyên phát gia đình với tăng calci niệu và nhiễm calci thận mà không có liên quan đến mắt nặng
900000000000448009 |Entire term case insensitive (core metadata concept)|
None
True

3446858016 - Familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (en) View

3446858016
en
Synonym (core metadata concept)
Familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis without severe ocular involvement
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3446857014 - Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (en) View

3446857014
en
Synonym (core metadata concept)
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3446856017 - Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (disorder) (en) View

3446856017
en
Fully specified name (core metadata concept)
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3446860019 - Renal hypomagnesaemia type 3 (en) View

3446860019
en
Synonym (core metadata concept)
Renal hypomagnesaemia type 3
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

3446859012 - Renal hypomagnesemia type 3 (en) View

3446859012
en
Synonym (core metadata concept)
Renal hypomagnesemia type 3
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

Relationship (16198186028) - 725033008 -> 73668004 (363714003) View

363714003 |Interprets (attribute)|
73668004 |Calcium measurement, urine (procedure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (16198187021) - 725033008 -> 281302008 (363713009) View

363713009 |Has interpretation (attribute)|
281302008 |Above reference range (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6872544028) - 725033008 -> 50029007 (116680003) View

116680003 |Is a (attribute)|
50029007 |Familial hypomagnesemia-hypercalciuria (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (6872545027) - 725033008 -> 85995004 (116680003) View

116680003 |Is a (attribute)|
85995004 |Autosomal recessive hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (6915464029) - 725033008 -> 48638002 (116680003) View

116680003 |Is a (attribute)|
48638002 |Nephrocalcinosis (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (6915465028) - 725033008 -> 367591000119105 (116680003) View

116680003 |Is a (attribute)|
367591000119105 |Hereditary nephropathy (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (15905466021) - 725033008 -> 1304111007 (116680003) View

116680003 |Is a (attribute)|
1304111007 |Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6915467020) - 725033008 -> 64033007 (363698007) View

363698007 |Finding site (attribute)|
64033007 |Kidney structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (15627045025) - 725033008 -> 29704000 (363698007) View

363698007 |Finding site (attribute)|
29704000 |Structure of parenchyma of kidney (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6915466027) - 725033008 -> 18115005 (116676008) View

116676008 |Associated morphology (attribute)|
18115005 |Pathologic calcification, calcified structure (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

1304111007 View

1304111007
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis (disorder)
Michellis castrillo syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (9b4bd9a7-f93d-5186-8de9-507926dce0d0) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
E83.5
TRUE
ALWAYS E83.5
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 (ea89b8eb-7ef7-52d6-bec6-c490cb882430) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
E83.4
TRUE
ALWAYS E83.4 | 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)|
447637006 |Map source concept is properly classified (foundation metadata concept)|

ExtendedMap object (f003d57e-b150-5be8-b97b-288bf1c4e585) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
N29.8
TRUE
ALWAYS N29.8 | THIS CODE MAY BE USED IN THE PRIMARY POSITION WHEN THE MANIFESTATION IS THE PRIMARY FOCUS OF CARE
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)|
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