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Terminology chevron_right Concepts chevron_right 429962007

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Component

429962007

The component that hold information about this concept.

Fully Specified Name (FSN)

Family history of hereditary disease (situation)

Shortest Term

Family history of genetic disease

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

Family history of hereditary disease (situation)

SCTID: 429962007, Defined, Active

429962007|Family history of hereditary disease (situation)|

vi Tiền sử gia đình mắc bệnh di truyền
vi Tiền sử gia đình mắc bệnh di truyền
en Family history of genetic disease
en Family history of hereditary disease
en Family history of hereditary disease (situation)
en Family history of heritable disorder

Expression

429962007 |Family history of hereditary disease (situation)|
 === 281666001 |Family history of disorder (situation)| : 
        { 246090004 |Associated finding (attribute)| = 32895009 |Hereditary disease (disorder)|,
408729009 |Finding context (attribute)| = 410515003 |Known present (qualifier value)|,
408732007 |Subject relationship context (attribute)| = 303071001 |Person in the family (person)|,
408731000 |Temporal context (attribute)| = 410511007 |Current or past (actual) (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
474281000003111 - tiền sử gia đình mắc bệnh di truyền (vi) View
474281000003111	vi	Synonym (core metadata concept)	tiền sử gia đình mắc bệnh di truyền	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	None	True
505771000003117 - tiền sử gia đình mắc bệnh di truyền (vi) View
505771000003117	vi	Synonym (core metadata concept)	tiền sử gia đình mắc bệnh di truyền	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2764084012 - Family history of genetic disease (en) View
2764084012	en	Synonym (core metadata concept)	Family history of genetic disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
2764338014 - Family history of hereditary disease (en) View
2764338014	en	Synonym (core metadata concept)	Family history of hereditary disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2708385018 - Family history of hereditary disease (situation) (en) View
2708385018	en	Fully specified name (core metadata concept)	Family history of hereditary disease (situation)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3035781016 - Family history of heritable disorder (en) View
3035781016	en	Synonym (core metadata concept)	Family history of heritable disorder	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (3534516025) - 429962007 -> 303071001 (408732007) View
408732007 \|Subject relationship context (attribute)\|	303071001 \|Person in the family (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3785965023) - 429962007 -> 444148008 (408732007) View
408732007 \|Subject relationship context (attribute)\|	444148008 \|Person in family of subject (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3534517023) - 429962007 -> 32895009 (246090004) View
246090004 \|Associated finding (attribute)\|	32895009 \|Hereditary disease (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3534518029) - 429962007 -> 410515003 (408729009) View
408729009 \|Finding context (attribute)\|	410515003 \|Known present (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3660576024) - 429962007 -> 410511007 (408731000) View
408731000 \|Temporal context (attribute)\|	410511007 \|Current or past (actual) (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3693430028) - 429962007 -> 32895009 (246090004) View
246090004 \|Associated finding (attribute)\|	32895009 \|Hereditary disease (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3693431029) - 429962007 -> 410515003 (408729009) View
408729009 \|Finding context (attribute)\|	410515003 \|Known present (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3693432020) - 429962007 -> 444148008 (408732007) View
408732007 \|Subject relationship context (attribute)\|	444148008 \|Person in family of subject (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3789201029) - 429962007 -> 410511007 (408731000) View
408731000 \|Temporal context (attribute)\|	410511007 \|Current or past (actual) (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3534519021) - 429962007 -> 410512000 (408731000) View
408731000 \|Temporal context (attribute)\|	410512000 \|Current or specified time (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3413362026) - 429962007 -> 410515003 (408729009) View
408729009 \|Finding context (attribute)\|	410515003 \|Known present (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3486198027) - 429962007 -> 32895009 (246090004) View
246090004 \|Associated finding (attribute)\|	32895009 \|Hereditary disease (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3486199024) - 429962007 -> 410512000 (408731000) View
408731000 \|Temporal context (attribute)\|	410512000 \|Current or specified time (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3486200022) - 429962007 -> 303071001 (408732007) View
408732007 \|Subject relationship context (attribute)\|	303071001 \|Person in the family (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3283247022) - 429962007 -> 281666001 (116680003) View
116680003 \|Is a (attribute)\|	281666001 \|Family history of disorder (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
281666001 View
281666001	Family history of disorder (situation)	Tiền sử gia đình mắc bệnh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
218432961000119106 View
218432961000119106	Family history of hereditary diffuse carcinoma of stomach (situation)	Family history of hereditary diffuse gastric cancer	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
64171000119108 View
64171000119108	Family history of lysosomal storage disease (situation)	Family history of lysosomal storage disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1269318001 View
1269318001	Family history of congenital long qt syndrome (situation)	Family history of congenital long qt syndrome	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
109271000119105 View
109271000119105	Family history of double heterozygous familial hypercholesterolemia (situation)	Tiền sử gia đình tăng cholesterol máu gia đình dị hợp tử kép	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
81651000119109 View
81651000119109	Family history of heritable malignancy (situation)	Family history of heritable cancer	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
63881000119101 View
63881000119101	Family history of spinocerebellar ataxia (situation)	Family history of spinocerebellar ataxia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
63931000119106 View
63931000119106	Family history of steinert myotonic dystrophy (situation)	Family history of myotonic muscular dystrophy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
64391000119106 View
64391000119106	Family history of hemoglobinopathy e (situation)	Family history of hemoglobinopathy e	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
64971000119106 View
64971000119106	Family history of von hippel-lindau syndrome (situation)	Tiền sử gia đình hội chứng von hippel-lindau	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
65031000119108 View
65031000119108	Family history of cowden syndrome (situation)	Tiền sử gia đình hội chứng cowden	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
109011000119108 View
109011000119108	Family history of protein c resistance (situation)	Tiền sử gia đình kháng protein c	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
709090007 View
709090007	Family history of familial multiple polyposis syndrome (situation)	Tiền sử gia đình mắc hội chứng đa polyp gia đình	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
63921000119108 View
63921000119108	Family history of rett syndrome (situation)	Family history of rett syndrome	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
64121000119107 View
64121000119107	Family history of achondroplasia (situation)	Tiền sử gia đình loạn sản sụn	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
64161000119102 View
64161000119102	Family history of phenylketonuria (situation)	Family history of phenylketonuria	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
64181000119106 View
64181000119106	Family history of marfan syndrome (situation)	Family history of marfan syndrome	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
64251000119106 View
64251000119106	Family history of glycogen storage disease (situation)	Tiền sử gia đình mắc bệnh dự trữ glycogen	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
65071000119106 View
65071000119106	Family history of fragile x syndrome (situation)	Family history of fragile x syndrome	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
94691000119101 View
94691000119101	Family history of familial dysautonomia (situation)	Family history of familial dysautonomia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
98251000119101 View
98251000119101	Family history of spongy degeneration of central nervous system (situation)	Family history of canavan disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1098871000119109 View
1098871000119109	Family history of hereditary nonpolyposis colon cancer (situation)	Family history of hereditary nonpolyposis colon cancer	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
71271000119107 View
71271000119107	Family history of retinitis pigmentosa (situation)	Family history of retinitis pigmentosa	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
429970002 View
429970002	Family history of charcot-marie-tooth disease (situation)	Tiền sử gia đình mắc bệnh charcot-marie-tooth	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
431912005 View
431912005	Family history of alpha-1-antitrypsin deficiency (situation)	Tiền sử gia đình thiếu alpha-1-antitrypsin	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
417001009 View
417001009	Family history of tuberous sclerosis (situation)	Family history of tuberous sclerosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
160309002 View
160309002	Family history of cystic fibrosis (situation)	Fh: cystic fibrosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
160318000 View
160318000	Family history: hereditary spherocytosis (context-dependent category)	Fh: hereditary spherocytosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
160319008 View
160319008	Family history: thalassemia (context-dependent category)	Fh: thalassemia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
160320002 View
160320002	Family history of sickle cell anemia (situation)	Fh: sickle cell anemia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
160321003 View
160321003	Family history: sickle cell trait (context-dependent category)	Fh: sickle cell trait	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
160336000 View
160336000	Family history: huntington's chorea (context-dependent category)	Fh: huntington's chorea	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 (280b399e-5faa-5e7b-b298-5b1375393a8e) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z84.8	TRUE	ALWAYS Z84.8	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)\|
ExtendedMap object (402d9bb2-14be-53d6-978a-924ccb6f83a1) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z82.7	IFA 417001009 \| Family history of tuberous sclerosis (situation) \|	IF FAMILY HISTORY OF TUBEROUS SCLEROSIS CHOOSE Z82.7 \| 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 (444c0ce9-a3e7-5de7-aa12-7410c362bc2b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z83.4	IFA 160312004 \| Family history: Cholinesterase deficiency (situation) \|	IF FAMILY HISTORY: CHOLINESTERASE DEFICIENCY CHOOSE Z83.4 \| 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 (46955b87-04d4-5edd-b060-f65478b48345) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z83.2	IFA 160318000 \| Family history: Hereditary spherocytosis (situation) \|	IF FAMILY HISTORY: HEREDITARY SPHEROCYTOSIS CHOOSE Z83.2 \| 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 (771a321b-6b8e-5d36-90b0-fe83ed2d3213) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z83.4	IFA 431912005 \| Family history of alpha-1-antitrypsin deficiency (situation) \|	IF FAMILY HISTORY OF ALPHA-1-ANTITRYPSIN DEFICIENCY CHOOSE Z83.4 \| 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 (781e0490-21e3-52cf-bbd9-ff7c1b3d885d) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z84.8	OTHERWISE TRUE	ALWAYS Z84.8	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)\|
ExtendedMap object (8f28c4dc-5884-50c5-af0d-335718bce371) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z83.5	IFA 71271000119107 \| Family history of retinitis pigmentosa (situation) \|	IF FAMILY HISTORY OF RETINITIS PIGMENTOSA CHOOSE Z83.5 \| 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 (a2a0da21-0a15-5a66-a42f-4ef5db738415) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z83.2	IFA 160319008 \| Family history: Thalassemia (situation) \|	IF FAMILY HISTORY: THALASSEMIA CHOOSE Z83.2 \| 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 (a9841c50-9475-5613-91a6-13fdc93e146d) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z83.2	IFA 160320002 \| Family history: Sickle cell anemia (situation) \|	IF FAMILY HISTORY: SICKLE CELL ANEMIA CHOOSE Z83.2 \| 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 (b5d694b0-d7e9-5d11-a0e8-9aea89dcf4bb) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z82.0	IFA 429970002 \| Family history of Charcot-Marie-Tooth disease (situation) \|	IF FAMILY HISTORY OF CHARCOT-MARIE-TOOTH DISEASE CHOOSE Z82.0 \| 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 (d1b48649-2c3a-5b14-9dc7-cf861e74d0c2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z83.2	IFA 160321003 \| Family history: Sickle cell trait (situation) \|	IF FAMILY HISTORY: SICKLE CELL TRAIT CHOOSE Z83.2 \| 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)\|

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (280b399e-5faa-5e7b-b298-5b1375393a8e) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z84.8	TRUE	ALWAYS Z84.8	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)\|
ExtendedMap object (402d9bb2-14be-53d6-978a-924ccb6f83a1) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z82.7	IFA 417001009 \| Family history of tuberous sclerosis (situation) \|	IF FAMILY HISTORY OF TUBEROUS SCLEROSIS CHOOSE Z82.7 \| 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 (444c0ce9-a3e7-5de7-aa12-7410c362bc2b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z83.4	IFA 160312004 \| Family history: Cholinesterase deficiency (situation) \|	IF FAMILY HISTORY: CHOLINESTERASE DEFICIENCY CHOOSE Z83.4 \| 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 (46955b87-04d4-5edd-b060-f65478b48345) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z83.2	IFA 160318000 \| Family history: Hereditary spherocytosis (situation) \|	IF FAMILY HISTORY: HEREDITARY SPHEROCYTOSIS CHOOSE Z83.2 \| 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 (771a321b-6b8e-5d36-90b0-fe83ed2d3213) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z83.4	IFA 431912005 \| Family history of alpha-1-antitrypsin deficiency (situation) \|	IF FAMILY HISTORY OF ALPHA-1-ANTITRYPSIN DEFICIENCY CHOOSE Z83.4 \| 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 (781e0490-21e3-52cf-bbd9-ff7c1b3d885d) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z84.8	OTHERWISE TRUE	ALWAYS Z84.8	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)\|
ExtendedMap object (8f28c4dc-5884-50c5-af0d-335718bce371) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z83.5	IFA 71271000119107 \| Family history of retinitis pigmentosa (situation) \|	IF FAMILY HISTORY OF RETINITIS PIGMENTOSA CHOOSE Z83.5 \| 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 (a2a0da21-0a15-5a66-a42f-4ef5db738415) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z83.2	IFA 160319008 \| Family history: Thalassemia (situation) \|	IF FAMILY HISTORY: THALASSEMIA CHOOSE Z83.2 \| 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 (a9841c50-9475-5613-91a6-13fdc93e146d) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z83.2	IFA 160320002 \| Family history: Sickle cell anemia (situation) \|	IF FAMILY HISTORY: SICKLE CELL ANEMIA CHOOSE Z83.2 \| 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 (b5d694b0-d7e9-5d11-a0e8-9aea89dcf4bb) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z82.0	IFA 429970002 \| Family history of Charcot-Marie-Tooth disease (situation) \|	IF FAMILY HISTORY OF CHARCOT-MARIE-TOOTH DISEASE CHOOSE Z82.0 \| 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 (d1b48649-2c3a-5b14-9dc7-cf861e74d0c2) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z83.2	IFA 160321003 \| Family history: Sickle cell trait (situation) \|	IF FAMILY HISTORY: SICKLE CELL TRAIT CHOOSE Z83.2 \| 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)\|

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