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Terminology chevron_right Concepts chevron_right 38804009

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Component

38804009

The component that hold information about this concept.

Fully Specified Name (FSN)

Turner syndrome (disorder)

Shortest Term

Xo 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

Turner syndrome (disorder)

SCTID: 38804009, Primitive, Active

38804009|Turner syndrome (disorder)|

vi Hội chứng turner
en Gonadal dysgenesis syndrome
en Pterygolymphangiectasia syndrome
en Turner syndrome (disorder)
en Bonnevie-ullrich syndrome
en Ts - turner's syndrome
en Turner's syndrome
en Turner syndrome

Expression

38804009 |Turner syndrome (disorder)|
 <<< 254277006 |Sex chromosome abnormality - female phenotype (disorder)| + 
111312006 |Anomaly of chromosome x (disorder)|
        { 116676008 |Associated morphology (attribute)| = 107675007 |Chromosomal morphology (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 72837006 |Sex chromosome x (cell structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
556561000003115 - hội chứng Turner (vi) View
556561000003115	vi	Synonym (core metadata concept)	hội chứng Turner	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
65087010 - Gonadal dysgenesis syndrome (en) View
65087010	en	Synonym (core metadata concept)	Gonadal dysgenesis syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
65084015 - Pterygolymphangiectasia syndrome (en) View
65084015	en	Synonym (core metadata concept)	Pterygolymphangiectasia syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
491783015 - 45X0 - Turner's syndrome (en) View
491783015	en	Synonym (core metadata concept)	45X0 - Turner's syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
65088017 - 45, X syndrome (en) View
65088017	en	Synonym (core metadata concept)	45, X syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
491782013 - Karyotype 45, X (en) View
491782013	en	Synonym (core metadata concept)	Karyotype 45, X	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
491779015 - X0 - Turner's syndrome (en) View
491779015	en	Synonym (core metadata concept)	X0 - Turner's syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
65086018 - XO syndrome (en) View
65086018	en	Synonym (core metadata concept)	XO syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
491785010 - Testicular dysgenesis (en) View
491785010	en	Synonym (core metadata concept)	Testicular dysgenesis	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
491781018 - Testicular dysplasia (en) View
491781018	en	Synonym (core metadata concept)	Testicular dysplasia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
775137014 - Turner syndrome (disorder) (en) View
775137014	en	Fully specified name (core metadata concept)	Turner syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
65085019 - Bonnevie-Ullrich syndrome (en) View
65085019	en	Synonym (core metadata concept)	Bonnevie-Ullrich syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
491784014 - TS - Turner's syndrome (en) View
491784014	en	Synonym (core metadata concept)	TS - Turner's syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
491780017 - Turner's syndrome (en) View
491780017	en	Synonym (core metadata concept)	Turner's syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
65082016 - Turner syndrome (en) View
65082016	en	Synonym (core metadata concept)	Turner syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
65083014 - Turner syndrome, NOS (en) View
65083014	en	Synonym (core metadata concept)	Turner syndrome, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (3525188026) - 38804009 -> 107675007 (116676008) View
116676008 \|Associated morphology (attribute)\|	107675007 \|Chromosomal morphology (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5007721027) - 38804009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5010373024) - 38804009 -> 107673000 (116676008) View
116676008 \|Associated morphology (attribute)\|	107673000 \|Cellular and/or subcellular abnormality (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5010374029) - 38804009 -> 72837006 (363698007) View
363698007 \|Finding site (attribute)\|	72837006 \|Sex chromosome x (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5925438027) - 38804009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5925439024) - 38804009 -> 72837006 (363698007) View
363698007 \|Finding site (attribute)\|	72837006 \|Sex chromosome x (cell structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6046913028) - 38804009 -> 107675007 (116676008) View
116676008 \|Associated morphology (attribute)\|	107675007 \|Chromosomal morphology (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (768813022) - 38804009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3525187020) - 38804009 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2595254023) - 38804009 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2595255024) - 38804009 -> 107675007 (116676008) View
116676008 \|Associated morphology (attribute)\|	107675007 \|Chromosomal morphology (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3093638020) - 38804009 -> 72837006 (363698007) View
363698007 \|Finding site (attribute)\|	72837006 \|Sex chromosome x (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3093639028) - 38804009 -> 72837006 (363698007) View
363698007 \|Finding site (attribute)\|	72837006 \|Sex chromosome x (cell structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2979357025) - 38804009 -> 72837006 (363698007) View
363698007 \|Finding site (attribute)\|	72837006 \|Sex chromosome x (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2979358024) - 38804009 -> 72837006 (363698007) View
363698007 \|Finding site (attribute)\|	72837006 \|Sex chromosome x (cell structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2914467020) - 38804009 -> 72837006 (363698007) View
363698007 \|Finding site (attribute)\|	72837006 \|Sex chromosome x (cell structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2914468026) - 38804009 -> 72837006 (363698007) View
363698007 \|Finding site (attribute)\|	72837006 \|Sex chromosome x (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2821564028) - 38804009 -> 72837006 (363698007) View
363698007 \|Finding site (attribute)\|	72837006 \|Sex chromosome x (cell structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2821565027) - 38804009 -> 72837006 (363698007) View
363698007 \|Finding site (attribute)\|	72837006 \|Sex chromosome x (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2674576028) - 38804009 -> 72837006 (363698007) View
363698007 \|Finding site (attribute)\|	72837006 \|Sex chromosome x (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2674577021) - 38804009 -> 72837006 (363698007) View
363698007 \|Finding site (attribute)\|	72837006 \|Sex chromosome x (cell structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (768815026) - 38804009 -> 72837006 (363698007) View
363698007 \|Finding site (attribute)\|	72837006 \|Sex chromosome x (cell structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2523948024) - 38804009 -> 72837006 (363698007) View
363698007 \|Finding site (attribute)\|	72837006 \|Sex chromosome x (cell structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (768814027) - 38804009 -> 41669009 (116676008) View
116676008 \|Associated morphology (attribute)\|	41669009 \|Alteration of chromosome structure (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2461698020) - 38804009 -> 399902003 (116680003) View
116680003 \|Is a (attribute)\|	399902003 \|Disorder of body cavity (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2461699028) - 38804009 -> 363124003 (116680003) View
116680003 \|Is a (attribute)\|	363124003 \|Disorder of female reproductive system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2461700027) - 38804009 -> 118948005 (116680003) View
116680003 \|Is a (attribute)\|	118948005 \|Disorder of abdomen (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2485972026) - 38804009 -> 15497006 (363698007) View
363698007 \|Finding site (attribute)\|	15497006 \|Ovarian structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (768812028) - 38804009 -> 40689003 (363698007) View
363698007 \|Finding site (attribute)\|	40689003 \|Testis structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2014993026) - 38804009 -> 64910008 (116680003) View
116680003 \|Is a (attribute)\|	64910008 \|Disorder of testis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1674270020) - 38804009 -> 64557000 (116680003) View
116680003 \|Is a (attribute)\|	64557000 \|Disorder of male genital organ (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (211081028) - 38804009 -> 126763008 (116680003) View
116680003 \|Is a (attribute)\|	126763008 \|Congenital anomaly of perineum (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (211082024) - 38804009 -> 42030000 (116680003) View
116680003 \|Is a (attribute)\|	42030000 \|Disorder of the genitourinary system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (211083025) - 38804009 -> 362968007 (116680003) View
116680003 \|Is a (attribute)\|	362968007 \|Disorder of reproductive system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (211079025) - 38804009 -> 254277006 (116680003) View
116680003 \|Is a (attribute)\|	254277006 \|Sex chromosome abnormality - female phenotype (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (211080027) - 38804009 -> 111312006 (116680003) View
116680003 \|Is a (attribute)\|	111312006 \|Anomaly of chromosome x (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
111312006 View
111312006	Anomaly of chromosome x (disorder)	Anomaly of chromosome x	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
254277006 View
254277006	Sex chromosome abnormality - female phenotype (disorder)	Sex chromosome abnormality - female phenotype	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
710008008 View
710008008	Monosomy x (disorder)	Monosomy x	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
710010005 View
710010005	Mosaic turner syndrome (disorder)	Mosaic turner syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
205684007 View
205684007	Turner's phenotype, karyotype normal (disorder)	Turner phenotype, karyotype normal	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
205686009 View
205686009	Karyotype 46, x iso (xq) (disorder)	Karyotype 46, x iso (xq)	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
205687000 View
205687000	Karyotype 46, x with abnormal sex chromosome except iso (xq) (disorder)	Karyotype 46, x with abnormal sex chromosome except iso (xq)	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
254280007 View
254280007	Turner's phenotype, partial x deletion karyotype (disorder)	Turner phenotype, partial x deletion karyotype	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
254281006 View
254281006	Turner's phenotype - ring chromosome karyotype (disorder)	Turner phenotype - ring chromosome karyotype	900000000000074008 \|Necessary but not sufficient concept 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 (3bd1c917-862c-5892-81fb-e45ed98028e3) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.8	IFA 254280007 \| Turner's phenotype, partial X deletion karyotype (disorder) \|	IF TURNER'S PHENOTYPE, PARTIAL X DELETION KARYOTYPE CHOOSE Q96.8 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (3ccefa2e-fb5f-54ba-aef6-d1f24a0bd34b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.1	IFA 205686009 \| Karyotype 46, X iso (Xq) (disorder) \|	IF KARYOTYPE 46, X ISO (XQ) CHOOSE Q96.1 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (57ee08d3-1f3a-5170-8339-d7c1780202f2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.8	IFA 254281006 \| Turner's phenotype - ring chromosome karyotype (disorder) \|	IF TURNER'S PHENOTYPE - RING CHROMOSOME KARYOTYPE CHOOSE Q96.8 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (5ed09c88-5c83-5799-95a5-6c7bfa0b9ef3) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.3	IFA 205688005 \| Turner's phenotype, mosaicism 45, X; 46, XX or 45, X; 46, XY (disorder) \|	IF TURNER'S PHENOTYPE, MOSAICISM 45, X; 46, XX OR 45, X; 46, XY CHOOSE Q96.3 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (9297760f-89f4-5781-922e-6f5e2d8dd88c) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.3	IFA 83579008 \| Mixed gonadal dysgenesis (disorder) \|	IF MIXED GONADAL DYSGENESIS CHOOSE Q96.3 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (a218786b-8d34-5075-894c-7661edc89ea9) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.2	IFA 205687000 \| Karyotype 46, X with abnormal sex chromosome except iso (Xq) (disorder) \|	IF KARYOTYPE 46, X WITH ABNORMAL SEX CHROMOSOME EXCEPT ISO (XQ) CHOOSE Q96.2 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (bb1ca769-2f90-5866-aaf2-cce118edd4ca) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.4	IFA 205689002 \| Mosaicism 45, X / other cell line with abnormal sex chromosome (disorder) \|	IF MOSAICISM 45, X / OTHER CELL LINE WITH ABNORMAL SEX CHROMOSOME CHOOSE Q96.4 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (c8a25754-910b-55cb-900d-0f480635434d) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.8	IFA 205684007 \| Turner's phenotype, karyotype normal (disorder) \|	IF TURNER'S PHENOTYPE, KARYOTYPE NORMAL CHOOSE Q96.8 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (ce25e739-ae6c-53a6-81fa-8ed454cea280) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.9	TRUE	ALWAYS Q96.9	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 (e5f8451f-6629-5221-bcb8-bf9b6115e938) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.3	IFA 302960008 \| Mosaicism 45, X; 46, XX (disorder) \|	IF MOSAICISM 45, X; 46, XX CHOOSE Q96.3 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (f89d8940-8c37-5121-a7d2-0b9d553f0337) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.9	OTHERWISE TRUE	ALWAYS Q96.9	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)\|

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (3bd1c917-862c-5892-81fb-e45ed98028e3) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.8	IFA 254280007 \| Turner's phenotype, partial X deletion karyotype (disorder) \|	IF TURNER'S PHENOTYPE, PARTIAL X DELETION KARYOTYPE CHOOSE Q96.8 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (3ccefa2e-fb5f-54ba-aef6-d1f24a0bd34b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.1	IFA 205686009 \| Karyotype 46, X iso (Xq) (disorder) \|	IF KARYOTYPE 46, X ISO (XQ) CHOOSE Q96.1 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (57ee08d3-1f3a-5170-8339-d7c1780202f2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.8	IFA 254281006 \| Turner's phenotype - ring chromosome karyotype (disorder) \|	IF TURNER'S PHENOTYPE - RING CHROMOSOME KARYOTYPE CHOOSE Q96.8 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (5ed09c88-5c83-5799-95a5-6c7bfa0b9ef3) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.3	IFA 205688005 \| Turner's phenotype, mosaicism 45, X; 46, XX or 45, X; 46, XY (disorder) \|	IF TURNER'S PHENOTYPE, MOSAICISM 45, X; 46, XX OR 45, X; 46, XY CHOOSE Q96.3 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (9297760f-89f4-5781-922e-6f5e2d8dd88c) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.3	IFA 83579008 \| Mixed gonadal dysgenesis (disorder) \|	IF MIXED GONADAL DYSGENESIS CHOOSE Q96.3 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (a218786b-8d34-5075-894c-7661edc89ea9) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.2	IFA 205687000 \| Karyotype 46, X with abnormal sex chromosome except iso (Xq) (disorder) \|	IF KARYOTYPE 46, X WITH ABNORMAL SEX CHROMOSOME EXCEPT ISO (XQ) CHOOSE Q96.2 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (bb1ca769-2f90-5866-aaf2-cce118edd4ca) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.4	IFA 205689002 \| Mosaicism 45, X / other cell line with abnormal sex chromosome (disorder) \|	IF MOSAICISM 45, X / OTHER CELL LINE WITH ABNORMAL SEX CHROMOSOME CHOOSE Q96.4 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (c8a25754-910b-55cb-900d-0f480635434d) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.8	IFA 205684007 \| Turner's phenotype, karyotype normal (disorder) \|	IF TURNER'S PHENOTYPE, KARYOTYPE NORMAL CHOOSE Q96.8 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (ce25e739-ae6c-53a6-81fa-8ed454cea280) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.9	TRUE	ALWAYS Q96.9	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 (e5f8451f-6629-5221-bcb8-bf9b6115e938) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.3	IFA 302960008 \| Mosaicism 45, X; 46, XX (disorder) \|	IF MOSAICISM 45, X; 46, XX CHOOSE Q96.3 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (f89d8940-8c37-5121-a7d2-0b9d553f0337) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q96.9	OTHERWISE TRUE	ALWAYS Q96.9	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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