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Terminology chevron_right Concepts chevron_right 91902004

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Component

91902004

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital absence of parietal bone (disorder)

Shortest Term

Agenesis of parietal bone

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

Congenital absence of parietal bone (disorder)

SCTID: 91902004, Defined, Active

91902004|Congenital absence of parietal bone (disorder)|

en Agenesis of parietal bone
en Congenital absence of parietal bone
en Congenital absence of parietal bone (disorder)

Expression

91902004 |Congenital absence of parietal bone (disorder)|
 === 93015002 |Congenital anomaly of parietal bone (disorder)| + 
1145449007 |Aplasia of bone of cranium (disorder)| + 
95464003 |Congenital absence of cranial vault (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 782173000 |Agenesis (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 181794000 |Entire parietal bone (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
152247018 - Agenesis of parietal bone (en) View
152247018	en	Synonym (core metadata concept)	Agenesis of parietal bone	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
152246010 - Congenital absence of parietal bone (en) View
152246010	en	Synonym (core metadata concept)	Congenital absence of parietal bone	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
835314017 - Congenital absence of parietal bone (disorder) (en) View
835314017	en	Fully specified name (core metadata concept)	Congenital absence of parietal bone (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15001695021) - 91902004 -> 203923004 (116680003) View
116680003 \|Is a (attribute)\|	203923004 \|Acrania (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16411056022) - 91902004 -> 95464003 (116680003) View
116680003 \|Is a (attribute)\|	95464003 \|Congenital absence of cranial vault (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (298714022) - 91902004 -> 841002 (116680003) View
116680003 \|Is a (attribute)\|	841002 \|Congenital absence of skull bone (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16245348025) - 91902004 -> 1145449007 (116680003) View
116680003 \|Is a (attribute)\|	1145449007 \|Aplasia of bone of cranium (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4973733028) - 91902004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4991406025) - 91902004 -> 24924006 (363698007) View
363698007 \|Finding site (attribute)\|	24924006 \|Parietal bone structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5000912021) - 91902004 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6092242028) - 91902004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10530619020) - 91902004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11165641026) - 91902004 -> 782173000 (116676008) View
116676008 \|Associated morphology (attribute)\|	782173000 \|Agenesis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11165642022) - 91902004 -> 181794000 (363698007) View
363698007 \|Finding site (attribute)\|	181794000 \|Entire parietal bone (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (905758027) - 91902004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3389033023) - 91902004 -> 24924006 (363698007) View
363698007 \|Finding site (attribute)\|	24924006 \|Parietal bone structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3389034028) - 91902004 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (566842023) - 91902004 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (905759024) - 91902004 -> 24924006 (363698007) View
363698007 \|Finding site (attribute)\|	24924006 \|Parietal bone structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3189391027) - 91902004 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3213373020) - 91902004 -> 89546000 (363698007) View
363698007 \|Finding site (attribute)\|	89546000 \|Bone structure of cranium (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (298713027) - 91902004 -> 93015002 (116680003) View
116680003 \|Is a (attribute)\|	93015002 \|Congenital anomaly of parietal bone (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1145449007 View
1145449007	Aplasia of bone of cranium (disorder)	Cranial aplasia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
95464003 View
95464003	Congenital absence of cranial vault (disorder)	Acrania	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
93015002 View
93015002	Congenital anomaly of parietal bone (disorder)	Congenital anomaly of parietal bone	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 (090dc86b-f114-58d1-b3d5-2bf6fc626f6f) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q75.8	TRUE	ALWAYS Q75.8	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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