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Terminology chevron_right Concepts chevron_right 774150004

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Component

774150004

The component that hold information about this concept.

Fully Specified Name (FSN)

Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder)

Shortest Term

Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome

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

Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder)

SCTID: 774150004, Primitive, Active

774150004|Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder)|

en Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome
en Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder)

Expression

774150004 |Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder)|
 <<< 363070008 |Developmental hereditary disorder (disorder)| + 
82354003 |Multiple system malformation syndrome (disorder)| + 
363235000 |Hereditary disorder of nervous system (disorder)| + 
205425003 |Sacral agenesis (disorder)| + 
81042008 |Congenital anomaly of spinal cord (disorder)| + 
253098009 |Neural tube defect (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 60271003 |Neural tube structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 782173000 |Agenesis (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 1144761009 |Entire sacral vertebral column region (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 25723000 |Dysplasia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 1144746008 |Structure of sacral vertebral column region (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 2748008 |Spinal cord 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
3728147016 - Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (en) View
3728147016	en	Synonym (core metadata concept)	Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3728148014 - Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder) (en) View
3728148014	en	Fully specified name (core metadata concept)	Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (10624875023) - 774150004 -> 297173004 (363698007) View
363698007 \|Finding site (attribute)\|	297173004 \|Lumbosacral region of spine structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10624882022) - 774150004 -> 363212003 (116680003) View
116680003 \|Is a (attribute)\|	363212003 \|Hereditary disorder of musculoskeletal system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11151373022) - 774150004 -> 264186006 (363698007) View
363698007 \|Finding site (attribute)\|	264186006 \|Entire sacral vertebral column (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13713316022) - 774150004 -> 1144746008 (363698007) View
363698007 \|Finding site (attribute)\|	1144746008 \|Structure of sacral vertebral column region (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13753210026) - 774150004 -> 81042008 (116680003) View
116680003 \|Is a (attribute)\|	81042008 \|Congenital anomaly of spinal cord (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13753726029) - 774150004 -> 1144761009 (363698007) View
363698007 \|Finding site (attribute)\|	1144761009 \|Entire sacral vertebral column region (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13070028028) - 774150004 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624867028) - 774150004 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624868022) - 774150004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624870029) - 774150004 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624871025) - 774150004 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624872021) - 774150004 -> 2748008 (363698007) View
363698007 \|Finding site (attribute)\|	2748008 \|Spinal cord structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624873027) - 774150004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624874022) - 774150004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624877026) - 774150004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624878020) - 774150004 -> 205425003 (116680003) View
116680003 \|Is a (attribute)\|	205425003 \|Sacral agenesis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624879028) - 774150004 -> 60271003 (363698007) View
363698007 \|Finding site (attribute)\|	60271003 \|Neural tube structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624880025) - 774150004 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624883028) - 774150004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624884023) - 774150004 -> 25723000 (116676008) View
116676008 \|Associated morphology (attribute)\|	25723000 \|Dysplasia (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624885024) - 774150004 -> 253098009 (116680003) View
116680003 \|Is a (attribute)\|	253098009 \|Neural tube defect (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624886020) - 774150004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624887027) - 774150004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624888021) - 774150004 -> 82354003 (116680003) View
116680003 \|Is a (attribute)\|	82354003 \|Multiple system malformation syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624889029) - 774150004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11151372028) - 774150004 -> 782173000 (116676008) View
116676008 \|Associated morphology (attribute)\|	782173000 \|Agenesis (morphologic abnormality)\|	2	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
253098009 View
253098009	Neural tube defect (disorder)	Neural tube defect	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
205425003 View
205425003	Sacral agenesis (disorder)	Sacral agenesis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
81042008 View
81042008	Congenital anomaly of spinal cord (disorder)	Deformity of spinal cord	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
82354003 View
82354003	Multiple system malformation syndrome (disorder)	Multiple system malformation syndrome	900000000000074008 \|Necessary but not sufficient concept 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 (4c0bbdbb-8f3a-57f6-8b33-1d2617806cc2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q87.5	TRUE	ALWAYS Q87.5 \| 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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