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Terminology chevron_right Concepts chevron_right 402786009

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402786009
The component that hold information about this concept.
Chylomicronemia syndrome (disorder)
Chylomicronemia syndrome
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

Chylomicronemia syndrome (disorder)

SCTID: 402786009, Primitive, Active


402786009|Chylomicronemia syndrome (disorder)|
  • en Chylomicronemia syndrome
  • en Chylomicronemia syndrome (disorder)

402786009 |Chylomicronemia syndrome (disorder)|

<<< 402726006 |Primary chylomicronemia (disorder)| +
    402785008 |Primary genetic hyperlipidemia (disorder)| :
        { 363713009 |Has interpretation (attribute)| = 281302008 |Above reference range (qualifier value)|,
          363714003 |Interprets (attribute)| = 104780002 |Lipids measurement (procedure)| }
Active

1781879012 - Chylomicronemia syndrome (en) View

1781879012
en
Synonym (core metadata concept)
Chylomicronemia syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

1770710014 - Chylomicronemia syndrome (disorder) (en) View

1770710014
en
Fully specified name (core metadata concept)
Chylomicronemia syndrome (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (4599213026) - 402786009 -> 124042003 (363705008) View

363705008 |Has definitional manifestation (attribute)|
124042003 |Increased lipid (finding)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (9358155021) - 402786009 -> 281302008 (363713009) View

363713009 |Has interpretation (attribute)|
281302008 |Above reference range (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (9358156022) - 402786009 -> 104780002 (363714003) View

363714003 |Interprets (attribute)|
104780002 |Lipids measurement (procedure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (3799672025) - 402786009 -> 166816003 (363705008) View

363705008 |Has definitional manifestation (attribute)|
166816003 |Serum lipids above reference range (finding)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (2288134021) - 402786009 -> 91689009 (363698007) View

363698007 |Finding site (attribute)|
91689009 |Body system structure (body structure)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (2248956021) - 402786009 -> 402726006 (116680003) View

116680003 |Is a (attribute)|
402726006 |Primary chylomicronemia (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (2248957028) - 402786009 -> 402785008 (116680003) View

116680003 |Is a (attribute)|
402785008 |Primary genetic hyperlipidemia (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

402726006 View

402726006
Primary chylomicronemia (disorder)
Primary chylomicronemia
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

402785008 View

402785008
Primary genetic hyperlipidemia (disorder)
Primary genetic hyperlipidemia
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

1197489003 View

1197489003
Familial chylomicronemia syndrome (disorder)
Familial chylomicronemia syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True
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