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Terminology chevron_right Concepts chevron_right 93015002

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Component

93015002

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital anomaly of parietal bone (disorder)

Shortest Term

Congenital anomaly 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 anomaly of parietal bone (disorder)

SCTID: 93015002, Defined, Active

93015002|Congenital anomaly of parietal bone (disorder)|

en Congenital anomaly of parietal bone
en Congenital anomaly of parietal bone (disorder)

Expression

93015002 |Congenital anomaly of parietal bone (disorder)|
 === 51655004 |Congenital anomaly of skull (disorder)| + 
298364001 |Finding of head region (finding)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 24924006 |Parietal bone 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
153847019 - Congenital anomaly of parietal bone (en) View
153847019	en	Synonym (core metadata concept)	Congenital anomaly of parietal bone	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
836660018 - Congenital anomaly of parietal bone (disorder) (en) View
836660018	en	Fully specified name (core metadata concept)	Congenital anomaly of parietal bone (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
153848012 - Congenital anomaly of parietal bone, NOS (en) View
153848012	en	Synonym (core metadata concept)	Congenital anomaly of parietal bone, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (913519025) - 93015002 -> 24924006 (363698007) View
363698007 \|Finding site (attribute)\|	24924006 \|Parietal bone structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4972463027) - 93015002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4972464022) - 93015002 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4989413026) - 93015002 -> 24924006 (363698007) View
363698007 \|Finding site (attribute)\|	24924006 \|Parietal bone structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6092774020) - 93015002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10530994025) - 93015002 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10530995029) - 93015002 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11178129023) - 93015002 -> 298364001 (116680003) View
116680003 \|Is a (attribute)\|	298364001 \|Finding of head region (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (301404021) - 93015002 -> 268239009 (116680003) View
116680003 \|Is a (attribute)\|	268239009 \|Congenital abnormality of skull and face bones (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (913518022) - 93015002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3314725024) - 93015002 -> 24924006 (363698007) View
363698007 \|Finding site (attribute)\|	24924006 \|Parietal bone structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3467018029) - 93015002 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4989412020) - 93015002 -> 51655004 (116680003) View
116680003 \|Is a (attribute)\|	51655004 \|Congenital anomaly of skull (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1783500023) - 93015002 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3197529026) - 93015002 -> 89546000 (363698007) View
363698007 \|Finding site (attribute)\|	89546000 \|Bone structure of cranium (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3200568021) - 93015002 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (301403026) - 93015002 -> 76069003 (116680003) View
116680003 \|Is a (attribute)\|	76069003 \|Disorder of bone (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
298364001 View
298364001	Finding of head region (finding)	Finding of head region	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
51655004 View
51655004	Congenital anomaly of skull (disorder)	Dị tật bẩm sinh của hộp sọ	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
253109005 View
253109005	Parietal encephalocele (disorder)	Parietal encephalocele	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
718099006 View
718099006	Enlarged parietal foramina (disorder)	Catlin marks	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
93596007 View
93596007	Incomplete ossification of parietal bone (disorder)	Reduced ossification of parietal bone	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
93112002 View
93112002	Lack of ossification of parietal bone (disorder)	Unossified parietal bone	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
91902004 View
91902004	Congenital absence of parietal bone (disorder)	Agenesis of parietal bone	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
92871009 View
92871009	Congenital abnormal fusion of parietal bone (disorder)	Congenital fused parietal bone	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
92936008 View
92936008	Congenital abnormal shape of parietal bone (disorder)	Congenital misshapen parietal bone	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
93085005 View
93085005	Congenital fenestration of parietal bone (disorder)	Congenital parietal hole	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
93282000 View
93282000	Congenital hypoplasia of parietal bone (disorder)	Congenital small parietal bone	900000000000073002 \|Sufficiently defined by necessary conditions 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 (85f01051-52cf-5abe-8c80-3cfec712b719) 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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