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Terminology chevron_right Concepts chevron_right 205707006

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Component

205707006

The component that hold information about this concept.

Fully Specified Name (FSN)

Mosaic xo/xy (disorder)

Shortest Term

Mosaic xo/xy

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

Mosaic xo/xy (disorder)

SCTID: 205707006, Primitive, Active

205707006|Mosaic xo/xy (disorder)|

en Mosaic xo/xy
en Mosaic xo/xy (disorder)

Expression

205707006 |Mosaic xo/xy (disorder)|
 <<< 205706002 |Sex chromosome mosaicism (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 8855009 |Mosaicism (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 312238009 |Chromosome 23 structure (cell structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
315471018 - Mosaic XO/XY (en) View
315471018	en	Synonym (core metadata concept)	Mosaic XO/XY	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
591112016 - Mosaic XO/XY (disorder) (en) View
591112016	en	Fully specified name (core metadata concept)	Mosaic XO/XY (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (5010402027) - 205707006 -> 32247007 (363698007) View
363698007 \|Finding site (attribute)\|	32247007 \|Sex chromosome (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16364537022) - 205707006 -> 312238009 (363698007) View
363698007 \|Finding site (attribute)\|	312238009 \|Chromosome 23 structure (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (971817027) - 205707006 -> 41669009 (116676008) View
116676008 \|Associated morphology (attribute)\|	41669009 \|Alteration of chromosome structure (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5010401023) - 205707006 -> 107673000 (116676008) View
116676008 \|Associated morphology (attribute)\|	107673000 \|Cellular and/or subcellular abnormality (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13796752023) - 205707006 -> 8855009 (116676008) View
116676008 \|Associated morphology (attribute)\|	8855009 \|Mosaicism (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (971814023) - 205707006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3435045023) - 205707006 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5007759024) - 205707006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3435044022) - 205707006 -> 32247007 (363698007) View
363698007 \|Finding site (attribute)\|	32247007 \|Sex chromosome (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (971815024) - 205707006 -> 32247007 (363698007) View
363698007 \|Finding site (attribute)\|	32247007 \|Sex chromosome (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2615827024) - 205707006 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (971816020) - 205707006 -> 302960008 (116676008) View
116676008 \|Associated morphology (attribute)\|	302960008 \|Mosaicism 45, x; 46, xx (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (331069024) - 205707006 -> 205706002 (116680003) View
116680003 \|Is a (attribute)\|	205706002 \|Sex chromosome mosaicism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
205706002 View
205706002	Sex chromosome mosaicism (disorder)	Sex chromosome mosaicism	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 (b2596161-d8d3-5bbd-aa7b-8d57e49e1a32) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.3	TRUE	ALWAYS Q96.3	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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