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Terminology chevron_right Concepts chevron_right 234446004

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234446004
The component that hold information about this concept.
Congenital von willebrand's disease (disorder)
Congenital von willebrand disease
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

Congenital von willebrand's disease (disorder)

SCTID: 234446004, Primitive, Inactive


234446004|Congenital von willebrand's disease (disorder)|
  • en Congenital von willebrand disease
  • en Congenital von willebrand's disease
  • en Congenital von willebrand's disease (disorder)
  • en Vwd - congenital von willebrand's disease

234446004 |Congenital von willebrand's disease (disorder)|

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Inactive

2839593011 - Congenital von Willebrand disease (en) View

2839593011
en
Synonym (core metadata concept)
Congenital von Willebrand disease
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

351268018 - Congenital von Willebrand's disease (en) View

351268018
en
Synonym (core metadata concept)
Congenital von Willebrand's disease
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

622765010 - Congenital von Willebrand's disease (disorder) (en) View

622765010
en
Fully specified name (core metadata concept)
Congenital von Willebrand's disease (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

351269014 - vWD - Congenital von Willebrand's disease (en) View

351269014
en
Synonym (core metadata concept)
vWD - Congenital von Willebrand's disease
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

Relationship (48122024) - 234446004 -> 128105004 (116680003) View

116680003 |Is a (attribute)|
128105004 |Von willebrand disorder (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (2532906027) - 234446004 -> 66091009 (116680003) View

116680003 |Is a (attribute)|
66091009 |Congenital disease (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (2573996021) - 234446004 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (11573553027) - 234446004 -> 263654008 (363713009) View

363713009 |Has interpretation (attribute)|
263654008 |Abnormal (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (11573554022) - 234446004 -> 74848003 (363714003) View

363714003 |Interprets (attribute)|
74848003 |Hemostatic function (observable entity)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (2712106022) - 234446004 -> 91689009 (363698007) View

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

Relationship (2778893025) - 234446004 -> 128153000 (363705008) View

363705008 |Has definitional manifestation (attribute)|
128153000 |Hemostatic system finding (finding)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (514080020) - 234446004 -> 281833003 (363698007) View

363698007 |Finding site (attribute)|
281833003 |Entire hematological system (body structure)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

ExtendedMap object (3d2b2ec4-faa2-52f8-84e8-ecced6602dcc) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
D68.0
TRUE
ALWAYS D68.0
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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