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Terminology chevron_right Concepts chevron_right 726381002

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726381002
The component that hold information about this concept.
Deletion of part of chromosome 11 (disorder)
Deletion of part of chromosome 11
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Deletion of part of chromosome 11 (disorder)

SCTID: 726381002, Defined, Active


726381002|Deletion of part of chromosome 11 (disorder)|
  • en Deletion of part of chromosome 11
  • en Deletion of part of chromosome 11 (disorder)

726381002 |Deletion of part of chromosome 11 (disorder)|

=== 60891003 |Anomaly of chromosome pair 11 (disorder)| +
    254274004 |Deletion of part of autosome (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 371169004 |Partial monosomy (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 16312006 |Chromosome pair 11 (cell structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
Active

3448832011 - Deletion of part of chromosome 11 (en) View

3448832011
en
Synonym (core metadata concept)
Deletion of part of chromosome 11
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3448831016 - Deletion of part of chromosome 11 (disorder) (en) View

3448831016
en
Fully specified name (core metadata concept)
Deletion of part of chromosome 11 (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

254274004 View

254274004
Deletion of part of autosome (disorder)
Deletion of part of autosome
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

60891003 View

60891003
Anomaly of chromosome pair 11 (disorder)
Anomaly of chromosome pair 11
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

4135001 View

4135001
11p partial monosomy syndrome (disorder)
11p partial monosomy syndrome
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

770944002 View

770944002
Oculootodental syndrome (disorder)
Oculootodental syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

715438008 View

715438008
Distal partial deletion of long arm of chromosome 11 (disorder)
Jacobsen syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

4325000 View

4325000
11q partial monosomy syndrome (disorder)
11q partial monosomy syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (8fd1eb87-2fd4-5643-865e-13611089faf5) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Q93.5
TRUE
ALWAYS Q93.5
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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