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Terminology chevron_right Concepts chevron_right 1003895007

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1003895007
The component that hold information about this concept.
Proximal deletion of long arm of chromosome 9 (disorder)
Proximal deletion of long arm of chromosome 9
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

Proximal deletion of long arm of chromosome 9 (disorder)

SCTID: 1003895007, Primitive, Active


1003895007|Proximal deletion of long arm of chromosome 9 (disorder)|
  • en Proximal deletion of long arm of chromosome 9
  • en Proximal deletion of long arm of chromosome 9 (disorder)

1003895007 |Proximal deletion of long arm of chromosome 9 (disorder)|

<<< 43420005 |9q partial monosomy syndrome (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 371169004 |Partial monosomy (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 13526007 |Chromosome pair 9 (cell structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 64329008 |Deletion of long arm (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 13526007 |Chromosome pair 9 (cell structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
Active

4166912016 - Proximal deletion of long arm of chromosome 9 (en) View

4166912016
en
Synonym (core metadata concept)
Proximal deletion of long arm of chromosome 9
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

4166911011 - Proximal deletion of long arm of chromosome 9 (disorder) (en) View

4166911011
en
Fully specified name (core metadata concept)
Proximal deletion of long arm of chromosome 9 (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (13189736028) - 1003895007 -> 43420005 (116680003) View

116680003 |Is a (attribute)|
43420005 |9q partial monosomy syndrome (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (13189737021) - 1003895007 -> 371169004 (116676008) View

116676008 |Associated morphology (attribute)|
371169004 |Partial monosomy (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (13189738027) - 1003895007 -> 13526007 (363698007) View

363698007 |Finding site (attribute)|
13526007 |Chromosome pair 9 (cell structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (13189739024) - 1003895007 -> 255399007 (246454002) View

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

Relationship (13189743023) - 1003895007 -> 13526007 (363698007) View

363698007 |Finding site (attribute)|
13526007 |Chromosome pair 9 (cell structure)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (13189744028) - 1003895007 -> 64329008 (116676008) View

116676008 |Associated morphology (attribute)|
64329008 |Deletion of long arm (morphologic abnormality)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (13189745027) - 1003895007 -> 255399007 (246454002) View

246454002 |Occurrence (attribute)|
255399007 |Congenital (qualifier value)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
True

43420005 View

43420005
9q partial monosomy syndrome (disorder)
9q partial monosomy syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (0b8abd74-7d2a-55e0-a716-9ed8133b7290) 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)|
esc