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Terminology chevron_right Concepts chevron_right 890130000

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890130000
The component that hold information about this concept.
9q34 deletion syndrome (disorder)
9q34 deletion 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

9q34 deletion syndrome (disorder)

SCTID: 890130000, Primitive, Active


890130000|9q34 deletion syndrome (disorder)|
  • en 9q34 deletion syndrome
  • en 9q34 deletion syndrome (disorder)

890130000 |9q34 deletion syndrome (disorder)|

<<< 43420005 |9q partial monosomy syndrome (disorder)| +
    276654001 |Congenital malformation (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)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (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)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
Active

4009227018 - 9q34 deletion syndrome (en) View

4009227018
en
Synonym (core metadata concept)
9q34 deletion syndrome
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

4009226010 - 9q34 deletion syndrome (disorder) (en) View

4009226010
en
Fully specified name (core metadata concept)
9q34 deletion syndrome (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

Relationship (12997578023) - 890130000 -> 43420005 (116680003) View

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

Relationship (12997579026) - 890130000 -> 276654001 (116680003) View

116680003 |Is a (attribute)|
276654001 |Congenital malformation (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (12997580028) - 890130000 -> 371169004 (116676008) View

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

Relationship (12997581029) - 890130000 -> 13526007 (363698007) View

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

Relationship (12997582020) - 890130000 -> 255399007 (246454002) View

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

Relationship (12997583026) - 890130000 -> 308490002 (370135005) View

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

Relationship (12997584021) - 890130000 -> 13526007 (363698007) View

363698007 |Finding site (attribute)|
13526007 |Chromosome pair 9 (cell structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (12997585022) - 890130000 -> 64329008 (116676008) View

116676008 |Associated morphology (attribute)|
64329008 |Deletion of long arm (morphologic abnormality)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (12997586023) - 890130000 -> 255399007 (246454002) View

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

Relationship (12997587025) - 890130000 -> 308490002 (370135005) View

370135005 |Pathological process (attribute)|
308490002 |Pathological developmental process (qualifier value)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
True

276654001 View

276654001
Congenital malformation (disorder)
Dị tật bẩm sinh
900000000000073002 |Sufficiently defined by necessary conditions definition status (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 (38ca610e-b5d7-5113-8178-51130d7060d4) 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