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Terminology chevron_right Concepts chevron_right 715817007

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Component

715817007

The component that hold information about this concept.

Fully Specified Name (FSN)

Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder)

Shortest Term

Lissencephaly with cerebellar hypoplasia

Definition Status

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

Summary

Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder)

SCTID: 715817007, Primitive, Active

715817007|Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder)|

en Lissencephaly co-occurrent with congenital cerebellar hypoplasia
en Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder)
en Lissencephaly with cerebellar hypoplasia

Expression

715817007 |Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder)|
 <<< 204036008 |Lissencephaly (disorder)| + 
16026008 |Congenital cerebellar hypoplasia (disorder)| + 
782964007 |Genetic disease (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)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3303804018 - Lissencephaly co-occurrent with congenital cerebellar hypoplasia (en) View
3303804018	en	Synonym (core metadata concept)	Lissencephaly co-occurrent with congenital cerebellar hypoplasia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3303801014 - Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder) (en) View
3303801014	en	Fully specified name (core metadata concept)	Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3303805017 - Lissencephaly with cerebellar hypoplasia (en) View
3303805017	en	Synonym (core metadata concept)	Lissencephaly with cerebellar hypoplasia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (12092540023) - 715817007 -> 782964007 (116680003) View
116680003 \|Is a (attribute)\|	782964007 \|Genetic disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6547463026) - 715817007 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6547464021) - 715817007 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6547465022) - 715817007 -> 55199003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55199003 \|Hypoplasia (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6547466023) - 715817007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6547467025) - 715817007 -> 113305005 (363698007) View
363698007 \|Finding site (attribute)\|	113305005 \|Cerebellar structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10529501021) - 715817007 -> 113305005 (363698007) View
363698007 \|Finding site (attribute)\|	113305005 \|Cerebellar structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10529502025) - 715817007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10529503024) - 715817007 -> 55199003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55199003 \|Hypoplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10529504029) - 715817007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6547461029) - 715817007 -> 16026008 (116680003) View
116680003 \|Is a (attribute)\|	16026008 \|Congenital cerebellar hypoplasia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6547462020) - 715817007 -> 204036008 (116680003) View
116680003 \|Is a (attribute)\|	204036008 \|Lissencephaly (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
782964007 View
782964007	Genetic disease (disorder)	Genetic disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
16026008 View
16026008	Congenital cerebellar hypoplasia (disorder)	Cerebellar hypoplasia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
204036008 View
204036008	Lissencephaly (disorder)	Agyria	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
785306007 View
785306007	Lissencephaly co-occurrent with congenital cerebellar hypoplasia type e (disorder)	Lissencephaly with cerebellar hypoplasia type e	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
785307003 View
785307003	Lissencephaly co-occurrent with congenital cerebellar hypoplasia type a (disorder)	Lissencephaly with cerebellar hypoplasia type a	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
715819005 View
715819005	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)\|	True
715820004 View
715820004	Lissencephaly co-occurrent with congenital cerebellar hypoplasia type c (disorder)	Lissencephaly with cerebellar hypoplasia type c	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
715821000 View
715821000	Lissencephaly co-occurrent with congenital cerebellar hypoplasia type d (disorder)	Lissencephaly with cerebellar hypoplasia type d	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
715822007 View
715822007	Lissencephaly co-occurrent with congenital cerebellar hypoplasia type f (disorder)	Lissencephaly with cerebellar hypoplasia type f	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (6505022b-6057-5d12-93e2-f610ba78f4c8) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q04.3	TRUE	ALWAYS Q04.3	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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