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Terminology chevron_right Concepts chevron_right 156982008

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156982008
The component that hold information about this concept.
(congenital) or (acquired) anomaly: [msk] or [skeletal] (disorder)
(congenital) or (acquired) anomaly: [msk] or [skeletal]
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) or (acquired) anomaly: [msk] or [skeletal] (disorder)

SCTID: 156982008, Primitive, Inactive


156982008|(congenital) or (acquired) anomaly: [msk] or [skeletal] (disorder)|
  • en (congenital) or (acquired) anomaly: [msk] or [skeletal] (disorder)
  • en (congenital) or (acquired) anomaly: [msk] or [skeletal]

156982008 |(congenital) or (acquired) anomaly: [msk] or [skeletal] (disorder)|

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Inactive

2726721014 - (Congenital) or (acquired) anomaly: [msk] or [skeletal] (disorder) (en) View

2726721014
en
Fully specified name (core metadata concept)
(Congenital) or (acquired) anomaly: [msk] or [skeletal] (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

245003018 - (Congenital) or (acquired) anomaly: [msk] or [skeletal] (en) View

245003018
en
Synonym (core metadata concept)
(Congenital) or (acquired) anomaly: [msk] or [skeletal]
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

537482012 - (Congenital) or (acquired) anomaly: [msk] or [skeletal] (en) View

537482012
en
Fully specified name (core metadata concept)
(Congenital) or (acquired) anomaly: [msk] or [skeletal]
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
False
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