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Terminology chevron_right Concepts chevron_right 715819005

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715819005
The component that hold information about this concept.
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type b (disorder)
Lissencephaly with cerebellar hypoplasia type b
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

Lissencephaly co-occurrent with congenital cerebellar hypoplasia type b (disorder)

SCTID: 715819005, Primitive, Active


715819005|Lissencephaly co-occurrent with congenital cerebellar hypoplasia type b (disorder)|
  • en Lissencephaly co-occurrent with congenital cerebellar hypoplasia type b
  • en Lissencephaly co-occurrent with congenital cerebellar hypoplasia type b (disorder)
  • en Lissencephaly with cerebellar hypoplasia type b

715819005 |Lissencephaly co-occurrent with congenital cerebellar hypoplasia type b (disorder)|

<<< 715817007 |Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder)| :
        { 116676008 |Associated morphology (attribute)| = 55199003 |Hypoplasia (morphologic abnormality)|,
          363698007 |Finding site (attribute)| = 113305005 |Cerebellar structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
          370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
Active

3303809011 - Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (en) View

3303809011
en
Synonym (core metadata concept)
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Acceptable
True

3303808015 - Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (disorder) (en) View

3303808015
en
Fully specified name (core metadata concept)
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (disorder)
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

3303810018 - Lissencephaly with cerebellar hypoplasia type B (en) View

3303810018
en
Synonym (core metadata concept)
Lissencephaly with cerebellar hypoplasia type B
900000000000020002 |Only initial character case insensitive (core metadata concept)|
Preferred
True

Relationship (6547469027) - 715819005 -> 107656002 (116676008) View

116676008 |Associated morphology (attribute)|
107656002 |Congenital anomaly (morphologic abnormality)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (6547470026) - 715819005 -> 12738006 (363698007) View

363698007 |Finding site (attribute)|
12738006 |Brain structure (body structure)|
2
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (6547471027) - 715819005 -> 55199003 (116676008) View

116676008 |Associated morphology (attribute)|
55199003 |Hypoplasia (morphologic abnormality)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (6547472023) - 715819005 -> 255399007 (246454002) View

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

Relationship (6547473029) - 715819005 -> 113305005 (363698007) View

363698007 |Finding site (attribute)|
113305005 |Cerebellar structure (body structure)|
3
900000000000011006 |Inferred relationship (core metadata concept)|
False

Relationship (10529604022) - 715819005 -> 255399007 (246454002) View

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

Relationship (10529605023) - 715819005 -> 308490002 (370135005) View

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

Relationship (10529606024) - 715819005 -> 55199003 (116676008) View

116676008 |Associated morphology (attribute)|
55199003 |Hypoplasia (morphologic abnormality)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (10529607026) - 715819005 -> 113305005 (363698007) View

363698007 |Finding site (attribute)|
113305005 |Cerebellar structure (body structure)|
1
900000000000011006 |Inferred relationship (core metadata concept)|
True

Relationship (6547468024) - 715819005 -> 715817007 (116680003) View

116680003 |Is a (attribute)|
715817007 |Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder)|
0
900000000000011006 |Inferred relationship (core metadata concept)|
True

715817007 View

715817007
Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder)
Lissencephaly with cerebellar hypoplasia
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (b4ae3aca-709f-567e-bc37-9feb75bde87d) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
Q04.3
TRUE
ALWAYS Q04.3 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
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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