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Terminology chevron_right Concepts chevron_right 403756008

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Component

403756008

The component that hold information about this concept.

Fully Specified Name (FSN)

Aplasia cutis in trisomy 13 syndrome (disorder)

Shortest Term

Aplasia cutis in trisomy 13 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

Aplasia cutis in trisomy 13 syndrome (disorder)

SCTID: 403756008, Primitive, Active

403756008|Aplasia cutis in trisomy 13 syndrome (disorder)|

en Aplasia cutis in trisomy 13 syndrome
en Aplasia cutis in trisomy 13 syndrome (disorder)

Expression

403756008 |Aplasia cutis in trisomy 13 syndrome (disorder)|
 <<< 35484002 |Aplasia cutis congenita (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 45486003 |Aplasia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 119181002 |Skin part (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 47429007 |Associated with (attribute)| = 21111006 |Complete trisomy 13 syndrome (disorder)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
1782766014 - Aplasia cutis in Trisomy 13 syndrome (en) View
1782766014	en	Synonym (core metadata concept)	Aplasia cutis in Trisomy 13 syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
1771682013 - Aplasia cutis in Trisomy 13 syndrome (disorder) (en) View
1771682013	en	Fully specified name (core metadata concept)	Aplasia cutis in Trisomy 13 syndrome (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6030063026) - 403756008 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13186749021) - 403756008 -> 45486003 (116676008) View
116676008 \|Associated morphology (attribute)\|	45486003 \|Aplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2755604027) - 403756008 -> 21111006 (47429007) View
47429007 \|Associated with (attribute)\|	21111006 \|Complete trisomy 13 syndrome (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10516198026) - 403756008 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4973973028) - 403756008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4996998025) - 403756008 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5042148025) - 403756008 -> 88456007 (116676008) View
116676008 \|Associated morphology (attribute)\|	88456007 \|Congenital partial absence (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6030062020) - 403756008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6030064021) - 403756008 -> 119181002 (363698007) View
363698007 \|Finding site (attribute)\|	119181002 \|Skin part (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2290920023) - 403756008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3435322022) - 403756008 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3435323028) - 403756008 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2290923020) - 403756008 -> 24216005 (116676008) View
116676008 \|Associated morphology (attribute)\|	24216005 \|Congenital absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2755603022) - 403756008 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2250428026) - 403756008 -> 21111006 (116680003) View
116680003 \|Is a (attribute)\|	21111006 \|Complete trisomy 13 syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2290917026) - 403756008 -> 20795001 (363698007) View
363698007 \|Finding site (attribute)\|	20795001 \|Structure of skin region (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2290918020) - 403756008 -> 55401003 (363698007) View
363698007 \|Finding site (attribute)\|	55401003 \|Chromosome pair 13 (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2290919028) - 403756008 -> 78989007 (116676008) View
116676008 \|Associated morphology (attribute)\|	78989007 \|Trisomy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2519579024) - 403756008 -> 55401003 (363698007) View
363698007 \|Finding site (attribute)\|	55401003 \|Chromosome pair 13 (cell structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2641211024) - 403756008 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2290922026) - 403756008 -> 41669009 (116676008) View
116676008 \|Associated morphology (attribute)\|	41669009 \|Alteration of chromosome structure (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2290921022) - 403756008 -> 32247007 (363698007) View
363698007 \|Finding site (attribute)\|	32247007 \|Sex chromosome (cell structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2250427020) - 403756008 -> 35484002 (116680003) View
116680003 \|Is a (attribute)\|	35484002 \|Aplasia cutis congenita (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
35484002 View
35484002	Aplasia cutis congenita (disorder)	Cutis aplasia	900000000000074008 \|Necessary but not sufficient concept 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 (a7fe7a5c-00c9-5b95-b6f8-0107aeac2db8) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q91.7	TRUE	ALWAYS Q91.7	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 (c8ac2df3-4243-52f6-8b9a-21fcaff87a53) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q84.8	TRUE	ALWAYS Q84.8	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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