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Terminology chevron_right Concepts chevron_right 725393000

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725393000
The component that hold information about this concept.
Autosomal dominant primary hypomagnesemia with hypocalciuria (disorder)
Isolated renal magnesium wasting
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

Autosomal dominant primary hypomagnesemia with hypocalciuria (disorder)

SCTID: 725393000, Primitive, Active


725393000|Autosomal dominant primary hypomagnesemia with hypocalciuria (disorder)|
  • en Autosomal dominant primary hypomagnesaemia with hypocalciuria
  • en Autosomal dominant primary hypomagnesemia with hypocalciuria
  • en Autosomal dominant primary hypomagnesemia with hypocalciuria (disorder)
  • en Homg2 - renal hypomagnesaemia type 2
  • en Homg2 - renal hypomagnesemia type 2
  • en Isolated autosomal dominant hypomagnesaemia
  • en Isolated autosomal dominant hypomagnesemia
  • en Isolated renal magnesium wasting

725393000 |Autosomal dominant primary hypomagnesemia with hypocalciuria (disorder)|

<<< 11164009 |Autosomal dominant hereditary disorder (disorder)| +
    80710001 |Primary hypomagnesemia (disorder)| +
    86353007 |Hypocalciuria (disorder)|
Active

3441992015 - Autosomal dominant primary hypomagnesaemia with hypocalciuria (en) View

3441992015
en
Synonym (core metadata concept)
Autosomal dominant primary hypomagnesaemia with hypocalciuria
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3441991010 - Autosomal dominant primary hypomagnesemia with hypocalciuria (en) View

3441991010
en
Synonym (core metadata concept)
Autosomal dominant primary hypomagnesemia with hypocalciuria
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3441990011 - Autosomal dominant primary hypomagnesemia with hypocalciuria (disorder) (en) View

3441990011
en
Fully specified name (core metadata concept)
Autosomal dominant primary hypomagnesemia with hypocalciuria (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3441996017 - HOMG2 - renal hypomagnesaemia type 2 (en) View

3441996017
en
Synonym (core metadata concept)
HOMG2 - renal hypomagnesaemia type 2
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

3441994019 - HOMG2 - renal hypomagnesemia type 2 (en) View

3441994019
en
Synonym (core metadata concept)
HOMG2 - renal hypomagnesemia type 2
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

3441997014 - Isolated autosomal dominant hypomagnesaemia (en) View

3441997014
en
Synonym (core metadata concept)
Isolated autosomal dominant hypomagnesaemia
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

3441995018 - Isolated autosomal dominant hypomagnesemia (en) View

3441995018
en
Synonym (core metadata concept)
Isolated autosomal dominant hypomagnesemia
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

3441993013 - Isolated renal magnesium wasting (en) View

3441993013
en
Synonym (core metadata concept)
Isolated renal magnesium wasting
900000000000448009 |Entire term case insensitive (core metadata concept)|
Acceptable
True

Relationship (6892489024) - 725393000 -> 11164009 (116680003) View

116680003 |Is a (attribute)|
11164009 |Autosomal dominant hereditary disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6892490026) - 725393000 -> 80710001 (116680003) View

116680003 |Is a (attribute)|
80710001 |Primary hypomagnesemia (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6892491027) - 725393000 -> 86353007 (116680003) View

116680003 |Is a (attribute)|
86353007 |Hypocalciuria (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

11164009 View

11164009
Autosomal dominant hereditary disorder (disorder)
Ad - autosomal dominant
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

80710001 View

80710001
Primary hypomagnesemia (disorder)
Primary hypomagnesemia
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

86353007 View

86353007
Hypocalciuria (disorder)
Hypocalciuria
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True
esc