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Terminology chevron_right Concepts chevron_right 890286007

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Component

890286007

The component that hold information about this concept.

Fully Specified Name (FSN)

Bilateral frontoparietal polymicrogyria (disorder)

Shortest Term

Bilateral frontoparietal polymicrogyria

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

Bilateral frontoparietal polymicrogyria (disorder)

SCTID: 890286007, Primitive, Active

890286007|Bilateral frontoparietal polymicrogyria (disorder)|

en Bfpp - bilateral frontoparietal polymicrogyria
en Bilateral frontoparietal polymicrogyria
en Bilateral frontoparietal polymicrogyria (disorder)

Expression

890286007 |Bilateral frontoparietal polymicrogyria (disorder)|
 <<< 363235000 |Hereditary disorder of nervous system (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| + 
765757003 |Bilateral polymicrogyria (disorder)| + 
702628006 |Congenital anomaly of cerebrum (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 1303834006 |Abnormal smallness (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 16792007 |Structure of frontal lobe gyrus (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 1303834006 |Abnormal smallness (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 34709004 |Structure of parietal lobe gyrus (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
4012684013 - BFPP - bilateral frontoparietal polymicrogyria (en) View
4012684013	en	Synonym (core metadata concept)	BFPP - bilateral frontoparietal polymicrogyria	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
4011914015 - Bilateral frontoparietal polymicrogyria (en) View
4011914015	en	Synonym (core metadata concept)	Bilateral frontoparietal polymicrogyria	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4011913014 - Bilateral frontoparietal polymicrogyria (disorder) (en) View
4011913014	en	Fully specified name (core metadata concept)	Bilateral frontoparietal polymicrogyria (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15810623026) - 890286007 -> 298364001 (116680003) View
116680003 \|Is a (attribute)\|	298364001 \|Finding of head region (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13003346020) - 890286007 -> 41086002 (116676008) View
116676008 \|Associated morphology (attribute)\|	41086002 \|Congenital smallness (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13003373021) - 890286007 -> 41086002 (116676008) View
116676008 \|Associated morphology (attribute)\|	41086002 \|Congenital smallness (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15898952023) - 890286007 -> 1303834006 (116676008) View
116676008 \|Associated morphology (attribute)\|	1303834006 \|Abnormal smallness (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15898953029) - 890286007 -> 1303834006 (116676008) View
116676008 \|Associated morphology (attribute)\|	1303834006 \|Abnormal smallness (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13003370024) - 890286007 -> 128128003 (116680003) View
116680003 \|Is a (attribute)\|	128128003 \|Disorder of cerebral cortex (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13003342022) - 890286007 -> 765757003 (116680003) View
116680003 \|Is a (attribute)\|	765757003 \|Bilateral polymicrogyria (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13003344023) - 890286007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13003345024) - 890286007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13003371023) - 890286007 -> 702628006 (116680003) View
116680003 \|Is a (attribute)\|	702628006 \|Congenital anomaly of cerebrum (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13003372027) - 890286007 -> 16792007 (363698007) View
363698007 \|Finding site (attribute)\|	16792007 \|Structure of frontal lobe gyrus (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13003374026) - 890286007 -> 34709004 (363698007) View
363698007 \|Finding site (attribute)\|	34709004 \|Structure of parietal lobe gyrus (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13003375025) - 890286007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13003376029) - 890286007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13005283020) - 890286007 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13005284025) - 890286007 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13070058023) - 890286007 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
363070008 View
363070008	Developmental hereditary disorder (disorder)	Developmental hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
765757003 View
765757003	Bilateral polymicrogyria (disorder)	Bilateral polymicrogyria	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
702628006 View
702628006	Congenital anomaly of cerebrum (disorder)	Congenital anomaly of cerebrum	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363235000 View
363235000	Hereditary disorder of nervous system (disorder)	Hereditary disorder of nervous system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

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 (1d97e73d-728c-5316-9c7b-5434b23dfba1) 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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