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Terminology chevron_right Concepts chevron_right 129601002

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129601002
The component that hold information about this concept.
Congenital neurogenic ileus syndrome (disorder)
Jirasek-zuelzer-wilson 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

Congenital neurogenic ileus syndrome (disorder)

SCTID: 129601002, Primitive, Active


129601002|Congenital neurogenic ileus syndrome (disorder)|
  • en Jirasek-zuelzer-wilson syndrome
  • en Congenital neurogenic ileus syndrome
  • en Congenital neurogenic ileus syndrome (disorder)

129601002 |Congenital neurogenic ileus syndrome (disorder)|

<<< 81060008 |Intestinal obstruction (disorder)| +
    126764002 |Congenital anomaly of intestinal tract (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 26036001 |Obstruction (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 783798004 |Structure of lumen of intestine (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
Active

208409013 - Jirasek-Zuelzer-Wilson syndrome (en) View

208409013
en
Synonym (core metadata concept)
Jirasek-Zuelzer-Wilson syndrome
900000000000017005 |Entire term case sensitive (core metadata concept)|
Acceptable
True

208408017 - Congenital neurogenic ileus syndrome (en) View

208408017
en
Synonym (core metadata concept)
Congenital neurogenic ileus syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

733755018 - Congenital neurogenic ileus syndrome (disorder) (en) View

733755018
en
Fully specified name (core metadata concept)
Congenital neurogenic ileus syndrome (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (2558855022) - 129601002 -> 66091009 (116680003) View

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

Relationship (13692325029) - 129601002 -> 308490002 (370135005) View

370135005 |Pathological process (attribute)|
308490002 |Pathological developmental process (qualifier value)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (13692326028) - 129601002 -> 126764002 (116680003) View

116680003 |Is a (attribute)|
126764002 |Congenital anomaly of intestinal tract (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (1800127025) - 129601002 -> 26036001 (116676008) View

116676008 |Associated morphology (attribute)|
26036001 |Obstruction (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (5010820025) - 129601002 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (5010821026) - 129601002 -> 26036001 (116676008) View

116676008 |Associated morphology (attribute)|
26036001 |Obstruction (morphologic abnormality)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (5010822022) - 129601002 -> 113276009 (363698007) View

363698007 |Finding site (attribute)|
113276009 |Intestinal structure (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (12058202020) - 129601002 -> 255399007 (246454002) View

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

Relationship (12058203026) - 129601002 -> 783798004 (363698007) View

363698007 |Finding site (attribute)|
783798004 |Structure of lumen of intestine (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (2621201024) - 129601002 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (3399764025) - 129601002 -> 113276009 (363698007) View

363698007 |Finding site (attribute)|
113276009 |Intestinal structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (3399765029) - 129601002 -> 26036001 (116676008) View

116676008 |Associated morphology (attribute)|
26036001 |Obstruction (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (1800128024) - 129601002 -> 113276009 (363698007) View

363698007 |Finding site (attribute)|
113276009 |Intestinal structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (349896021) - 129601002 -> 81060008 (116680003) View

116680003 |Is a (attribute)|
81060008 |Intestinal obstruction (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

81060008 View

81060008
Intestinal obstruction (disorder)
Ileus
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

126764002 View

126764002
Congenital anomaly of intestinal tract (disorder)
Congenital anomaly of intestinal tract
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

ExtendedMap object (94b286e1-9e11-523f-9b69-d517b38c9d80) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Q43.1
TRUE
ALWAYS Q43.1
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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