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Terminology chevron_right Concepts chevron_right 1003374009

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Component

1003374009

The component that hold information about this concept.

Fully Specified Name (FSN)

Microlissencephaly (disorder)

Shortest Term

Microlissencephaly

Definition Status

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

Summary

Microlissencephaly (disorder)

SCTID: 1003374009, Defined, Active

1003374009|Microlissencephaly (disorder)|

en Microlissencephaly
en Microlissencephaly (disorder)

Expression

1003374009 |Microlissencephaly (disorder)|
 === 204036008 |Lissencephaly (disorder)| + 
1149087003 |Congenital microencephaly (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 1303834006 |Abnormal smallness (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 12738006 |Brain 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
4168105019 - Microlissencephaly (en) View
4168105019	en	Synonym (core metadata concept)	Microlissencephaly	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4168106018 - Microlissencephaly (disorder) (en) View
4168106018	en	Fully specified name (core metadata concept)	Microlissencephaly (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13185374025) - 1003374009 -> 41086002 (116676008) View
116676008 \|Associated morphology (attribute)\|	41086002 \|Congenital smallness (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15898959025) - 1003374009 -> 1303834006 (116676008) View
116676008 \|Associated morphology (attribute)\|	1303834006 \|Abnormal smallness (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13185370023) - 1003374009 -> 1829003 (116680003) View
116680003 \|Is a (attribute)\|	1829003 \|Microcephalus (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13745143025) - 1003374009 -> 1149087003 (116680003) View
116680003 \|Is a (attribute)\|	1149087003 \|Congenital microencephaly (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13185371022) - 1003374009 -> 204036008 (116680003) View
116680003 \|Is a (attribute)\|	204036008 \|Lissencephaly (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13185372026) - 1003374009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13185373020) - 1003374009 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13185375029) - 1003374009 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1149087003 View
1149087003	Congenital microencephaly (disorder)	Congenital microencephaly	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
718719001 View
718719001	Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder)	Lissencephaly type 3 familial fetal akinesia sequence syndrome	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 (698ace31-3b69-5f28-8381-567198caf2a3) 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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