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Terminology chevron_right Concepts chevron_right 597941000005106

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Component

597941000005106

The component that hold information about this concept.

Fully Specified Name (FSN)

Family history of congenital malformation (situation)

Shortest Term

Family history of congenital malformation

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 congenital malformation (situation)

SCTID: 597941000005106, Defined, Active

597941000005106|Family history of congenital malformation (situation)|

en Family history of congenital malformation
en Family history of congenital malformation (situation)

Expression

597941000005106 |Family history of congenital malformation (situation)|
 === 160417009 |Family history: congenital anomaly (situation)| + 
412749001 |Family history of development disorder (situation)| : 
        { 246090004 |Associated finding (attribute)| = 276654001 |Congenital malformation (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
5409931000005118 - Family history of congenital malformation (en) View
5409931000005118	en	Synonym (core metadata concept)	Family history of congenital malformation	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
5409941000005114 - Family history of congenital malformation (situation) (en) View
5409941000005114	en	Fully specified name (core metadata concept)	Family history of congenital malformation (situation)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (16019694021) - 597941000005106 -> 160417009 (116680003) View
116680003 \|Is a (attribute)\|	160417009 \|Family history: congenital anomaly (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16019695022) - 597941000005106 -> 412749001 (116680003) View
116680003 \|Is a (attribute)\|	412749001 \|Family history of development disorder (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16019696023) - 597941000005106 -> 276654001 (246090004) View
246090004 \|Associated finding (attribute)\|	276654001 \|Congenital malformation (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16019697025) - 597941000005106 -> 410515003 (408729009) View
408729009 \|Finding context (attribute)\|	410515003 \|Known present (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16019698024) - 597941000005106 -> 303071001 (408732007) View
408732007 \|Subject relationship context (attribute)\|	303071001 \|Person in the family (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16019699027) - 597941000005106 -> 410511007 (408731000) View
408731000 \|Temporal context (attribute)\|	410511007 \|Current or past (actual) (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
160417009 View
160417009	Family history: congenital anomaly (situation)	Fh: congenital anomaly	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
412749001 View
412749001	Family history of development disorder (situation)	Fh: development disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1148759006 View
1148759006	Family history of congenital microcephaly (situation)	Family history of congenital microcephaly	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
64731000119106 View
64731000119106	Family history of multiple congenital anomalies (situation)	Tiền sử gia đình đa dị tật bẩm sinh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
64841000119108 View
64841000119108	Family history of trisomy 18 (situation)	Family history of trisomy 18	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
63941000119102 View
63941000119102	Family history of congenital hydrocephalus (situation)	Tiền sử gia đình não úng thủy bẩm sinh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
64911000119103 View
64911000119103	Family history of cystic hygroma (situation)	Family history of cystic hygroma	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
85951000119104 View
85951000119104	Family history of single congenital anomaly (situation)	Tiền sử gia đình dị tật bẩm sinh đơn lẻ	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
429954004 View
429954004	Family history of cleft lip (situation)	Tiền sử gia đình sứt môi	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
429977004 View
429977004	Family history of congenital cataract (situation)	Family history of congenital cataract	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
430086009 View
430086009	Family history of cleft palate (situation)	Tiền sử gia đình hở hàm ếch	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
281022002 View
281022002	Down's child in family (situation)	Mongol child	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
160418004 View
160418004	Family history: anencephaly (context-dependent category)	Fh: anencephaly	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
160421002 View
160421002	Family history of congenital respiratory system anomaly (situation)	Fh: congenital rs anomaly	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
160422009 View
160422009	Family history: congenital gastrointestinal tract anomaly (context-dependent category)	Fh: congenital git anomaly	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
160423004 View
160423004	Family history: congenital genitourinary anomaly (situation)	Fh: congenital gu anomaly	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
160424005 View
160424005	Family history: congenital orthopedic anomaly (context-dependent category)	Fh: cong. orthopedic anomaly	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
266908007 View
266908007	Family history of congenital anomaly of cardiovascular system (situation)	Fh: congenital cvs anomaly	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 (1eaca4ff-3b79-5543-b8bf-02fa7e663560) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Z82.7	TRUE	ALWAYS Z82.7	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)\|

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