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Terminology chevron_right Concepts chevron_right 205794007

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205794007
The component that hold information about this concept.
(multiple system congenital anomalies nec) or (prader-willi syndrome) or (noonan's syndrome) (disorder)
Noonan's 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

(multiple system congenital anomalies nec) or (prader-willi syndrome) or (noonan's syndrome) (disorder)

SCTID: 205794007, Primitive, Inactive


205794007|(multiple system congenital anomalies nec) or (prader-willi syndrome) or (noonan's syndrome) (disorder)|
  • en (multiple system congenital anomalies nec) or (prader-willi syndrome) or (noonan's syndrome) (disorder)
  • en (multiple system congenital anomalies nec) or (prader-willi syndrome) or (noonan's syndrome)
  • en Multiple system congenital anomalies nec
  • en Noonan's syndrome
  • en Prader - willi syndrome
  • en Prader-willi syndrome
  • en Prader-willi syndrome

205794007 |(multiple system congenital anomalies nec) or (prader-willi syndrome) or (noonan's syndrome) (disorder)|

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Inactive

2750701016 - (Multiple system congenital anomalies NEC) or (Prader-Willi syndrome) or (Noonan's syndrome) (disorder) (en) View

2750701016
en
Fully specified name (core metadata concept)
(Multiple system congenital anomalies NEC) or (Prader-Willi syndrome) or (Noonan's syndrome) (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

315578014 - (Multiple system congenital anomalies NEC) or (Prader-Willi syndrome) or (Noonan's syndrome) (en) View

315578014
en
Synonym (core metadata concept)
(Multiple system congenital anomalies NEC) or (Prader-Willi syndrome) or (Noonan's syndrome)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

591211016 - (Multiple system congenital anomalies NEC) or (Prader-Willi syndrome) or (Noonan's syndrome) (en) View

591211016
en
Fully specified name (core metadata concept)
(Multiple system congenital anomalies NEC) or (Prader-Willi syndrome) or (Noonan's syndrome)
900000000000017005 |Entire term case sensitive (core metadata concept)|
Preferred
False

315582011 - Multiple system congenital anomalies NEC (en) View

315582011
en
Synonym (core metadata concept)
Multiple system congenital anomalies NEC
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

315583018 - Noonan's syndrome (en) View

315583018
en
Synonym (core metadata concept)
Noonan's syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

315581016 - Prader - Willi syndrome (en) View

315581016
en
Synonym (core metadata concept)
Prader - Willi syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

315580015 - Prader-Willi syndrome (en) View

315580015
en
Synonym (core metadata concept)
Prader-Willi syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

315579018 - Prader-Willi Syndrome (en) View

315579018
en
Synonym (core metadata concept)
Prader-Willi Syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True
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