Loading...
dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 722008003

Production
add
722008003
The component that hold information about this concept.
Isolated autosomal dominant hypomagnesemia glaudemans type (disorder)
Isolated autosomal dominant hypomagnesemia glaudemans type
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

Isolated autosomal dominant hypomagnesemia glaudemans type (disorder)

SCTID: 722008003, Primitive, Active


722008003|Isolated autosomal dominant hypomagnesemia glaudemans type (disorder)|
  • en Isolated autosomal dominant hypomagnesaemia glaudemans type
  • en Isolated autosomal dominant hypomagnesemia glaudemans type
  • en Isolated autosomal dominant hypomagnesemia glaudemans type (disorder)

722008003 |Isolated autosomal dominant hypomagnesemia glaudemans type (disorder)|

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

3330121010 - Isolated autosomal dominant hypomagnesaemia Glaudemans type (en) View

3330121010
en
Synonym (core metadata concept)
Isolated autosomal dominant hypomagnesaemia Glaudemans type
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

3313735011 - Isolated autosomal dominant hypomagnesemia Glaudemans type (en) View

3313735011
en
Synonym (core metadata concept)
Isolated autosomal dominant hypomagnesemia Glaudemans type
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

3313725017 - Isolated autosomal dominant hypomagnesemia Glaudemans type (disorder) (en) View

3313725017
en
Fully specified name (core metadata concept)
Isolated autosomal dominant hypomagnesemia Glaudemans type (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

Relationship (6778686023) - 722008003 -> 11164009 (116680003) View

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

Relationship (6778687025) - 722008003 -> 80710001 (116680003) View

116680003 |Is a (attribute)|
80710001 |Primary hypomagnesemia (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

ExtendedMap object (6b6e38c8-08ae-5735-a292-7bca2152d065) 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)|
esc