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Terminology chevron_right Concepts chevron_right 1829003

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Component

1829003

The component that hold information about this concept.

Fully Specified Name (FSN)

Microcephalus (disorder)

Shortest Term

Nanocephaly

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

Microcephalus (disorder)

SCTID: 1829003, Primitive, Inactive

1829003|Microcephalus (disorder)|

vi Chứng đầu nhỏ
en Micrencephaly
en Nanocephaly
en Microcephalus
en Microcephalus (disorder)
en Microcephaly

Expression

1829003 |Microcephalus (disorder)|
 <<< 

Diagram

Active

Inactive

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
598301000003117 - chứng đầu nhỏ (vi) View
598301000003117	vi	Synonym (core metadata concept)	chứng đầu nhỏ	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4161018 - Micrencephaly (en) View
4161018	en	Synonym (core metadata concept)	Micrencephaly	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
4162013 - Nanocephaly (en) View
4162013	en	Synonym (core metadata concept)	Nanocephaly	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
4159010 - Microcephalus (en) View
4159010	en	Synonym (core metadata concept)	Microcephalus	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
745690018 - Microcephalus (disorder) (en) View
745690018	en	Fully specified name (core metadata concept)	Microcephalus (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4160017 - Microcephaly (en) View
4160017	en	Synonym (core metadata concept)	Microcephaly	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (1669993024) - 1829003 -> 81308009 (116680003) View
116680003 \|Is a (attribute)\|	81308009 \|Disorder of brain (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6400116028) - 1829003 -> 41086002 (116676008) View
116676008 \|Associated morphology (attribute)\|	41086002 \|Congenital smallness (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6400117021) - 1829003 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4663134027) - 1829003 -> 230764002 (116680003) View
116680003 \|Is a (attribute)\|	230764002 \|Congenital and developmental anomalies of the nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4663133022) - 1829003 -> 41086002 (116676008) View
116676008 \|Associated morphology (attribute)\|	41086002 \|Congenital smallness (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4663135026) - 1829003 -> 258335003 (363698007) View
363698007 \|Finding site (attribute)\|	258335003 \|Entire brain (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (715925022) - 1829003 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (176123028) - 1829003 -> 253128003 (116680003) View
116680003 \|Is a (attribute)\|	253128003 \|Abnormality of neurogenesis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (715923026) - 1829003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (715924021) - 1829003 -> 41086002 (116676008) View
116676008 \|Associated morphology (attribute)\|	41086002 \|Congenital smallness (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (1d4ada07-ea16-51e4-8e34-8c5d43bd9396) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q04.4	IFA 77817004 \| Neu-Laxova syndrome (disorder) \|	IF NEU-LAXOVA SYNDROME CHOOSE Q04.4 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (1d7d42fd-2834-560c-abbf-d2e85e24bc42) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q87.8	IFA 703369003 \| Microcephaly-capillary malformation syndrome (disorder) \|	IF MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME CHOOSE Q87.8 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (3969e6f0-8728-598a-9849-a803474ebba5) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q02	TRUE	ALWAYS Q02	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)\|
ExtendedMap object (3b331d24-b094-5eeb-b1a3-04e142eb993b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q12.0	IFA 15552004 \| Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts (disorder) \|	IF OSTEOGENESIS IMPERFECTA, RECESSIVE PERINATAL LETHAL, WITH MICROCEPHALY AND CATARACTS CHOOSE Q12.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (69e00d99-2ea0-53be-a28c-91ddf603fc13) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q02	IFA 15552004 \| Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts (disorder) \|	IF OSTEOGENESIS IMPERFECTA, RECESSIVE PERINATAL LETHAL, WITH MICROCEPHALY AND CATARACTS CHOOSE Q02 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (6f5c1303-ebf7-535b-9e04-75a2e82d4fa0) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	OTHERWISE TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|
ExtendedMap object (b65351c2-8743-5c21-aca2-09f916efd861) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q02	OTHERWISE TRUE	ALWAYS Q02	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)\|
ExtendedMap object (b96a9b11-f764-5afb-8a2a-78520d90e1ea) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	OTHERWISE TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|
ExtendedMap object (d8e19d83-0271-5cb8-9583-af05974d9d80) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q78.8	IFA 389197004 \| Microcephalic osteodysplastic dysplasia (disorder) \|	IF MICROCEPHALIC OSTEODYSPLASTIC DYSPLASIA CHOOSE Q78.8 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (dac85c46-c63c-5e62-b305-505c77a77291) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q78.0	IFA 15552004 \| Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts (disorder) \|	IF OSTEOGENESIS IMPERFECTA, RECESSIVE PERINATAL LETHAL, WITH MICROCEPHALY AND CATARACTS CHOOSE Q78.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (1669993024) - 1829003 -> 81308009 (116680003) View
116680003 \|Is a (attribute)\|	81308009 \|Disorder of brain (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6400116028) - 1829003 -> 41086002 (116676008) View
116676008 \|Associated morphology (attribute)\|	41086002 \|Congenital smallness (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6400117021) - 1829003 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4663134027) - 1829003 -> 230764002 (116680003) View
116680003 \|Is a (attribute)\|	230764002 \|Congenital and developmental anomalies of the nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4663133022) - 1829003 -> 41086002 (116676008) View
116676008 \|Associated morphology (attribute)\|	41086002 \|Congenital smallness (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4663135026) - 1829003 -> 258335003 (363698007) View
363698007 \|Finding site (attribute)\|	258335003 \|Entire brain (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (715925022) - 1829003 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (176123028) - 1829003 -> 253128003 (116680003) View
116680003 \|Is a (attribute)\|	253128003 \|Abnormality of neurogenesis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (715923026) - 1829003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (715924021) - 1829003 -> 41086002 (116676008) View
116676008 \|Associated morphology (attribute)\|	41086002 \|Congenital smallness (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (1d4ada07-ea16-51e4-8e34-8c5d43bd9396) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q04.4	IFA 77817004 \| Neu-Laxova syndrome (disorder) \|	IF NEU-LAXOVA SYNDROME CHOOSE Q04.4 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (1d7d42fd-2834-560c-abbf-d2e85e24bc42) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q87.8	IFA 703369003 \| Microcephaly-capillary malformation syndrome (disorder) \|	IF MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME CHOOSE Q87.8 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (3969e6f0-8728-598a-9849-a803474ebba5) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q02	TRUE	ALWAYS Q02	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)\|
ExtendedMap object (3b331d24-b094-5eeb-b1a3-04e142eb993b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q12.0	IFA 15552004 \| Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts (disorder) \|	IF OSTEOGENESIS IMPERFECTA, RECESSIVE PERINATAL LETHAL, WITH MICROCEPHALY AND CATARACTS CHOOSE Q12.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (69e00d99-2ea0-53be-a28c-91ddf603fc13) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q02	IFA 15552004 \| Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts (disorder) \|	IF OSTEOGENESIS IMPERFECTA, RECESSIVE PERINATAL LETHAL, WITH MICROCEPHALY AND CATARACTS CHOOSE Q02 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (6f5c1303-ebf7-535b-9e04-75a2e82d4fa0) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	OTHERWISE TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|
ExtendedMap object (b65351c2-8743-5c21-aca2-09f916efd861) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q02	OTHERWISE TRUE	ALWAYS Q02	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)\|
ExtendedMap object (b96a9b11-f764-5afb-8a2a-78520d90e1ea) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	OTHERWISE TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|
ExtendedMap object (d8e19d83-0271-5cb8-9583-af05974d9d80) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q78.8	IFA 389197004 \| Microcephalic osteodysplastic dysplasia (disorder) \|	IF MICROCEPHALIC OSTEODYSPLASTIC DYSPLASIA CHOOSE Q78.8 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (dac85c46-c63c-5e62-b305-505c77a77291) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q78.0	IFA 15552004 \| Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts (disorder) \|	IF OSTEOGENESIS IMPERFECTA, RECESSIVE PERINATAL LETHAL, WITH MICROCEPHALY AND CATARACTS CHOOSE Q78.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|

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