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Terminology chevron_right Concepts chevron_right 199531009

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Component

199531009

The component that hold information about this concept.

Fully Specified Name (FSN)

Fetal hereditary disease (disorder)

Shortest Term

Fetal hereditary 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

Fetal hereditary disease (disorder)

SCTID: 199531009, Defined, Active

199531009|Fetal hereditary disease (disorder)|

en Fetal hereditary disease
en Fetal hereditary disease (disorder)
en Hereditary disorder of fetus
en Fetus with hereditary disease
en Foetus with hereditary disease

Expression

199531009 |Fetal hereditary disease (disorder)|
 === 32895009 |Hereditary disease (disorder)| + 
70591005 |Fetal disorder (disorder)| : 
        { 246454002 |Occurrence (attribute)| = 303112003 |Fetal period (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
5424615012 - Fetal hereditary disease (en) View
5424615012	en	Synonym (core metadata concept)	Fetal hereditary disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
5424616013 - Fetal hereditary disease (disorder) (en) View
5424616013	en	Fully specified name (core metadata concept)	Fetal hereditary disease (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
584171016 - Fetus with hereditary disease (disorder) (en) View
584171016	en	Fully specified name (core metadata concept)	Fetus with hereditary disease (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	False
5437930016 - Hereditary disorder of fetus (en) View
5437930016	en	Synonym (core metadata concept)	Hereditary disorder of fetus	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
306590012 - Fetus with hereditary disease (en) View
306590012	en	Synonym (core metadata concept)	Fetus with hereditary disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3011641019 - Foetus with hereditary disease (en) View
3011641019	en	Synonym (core metadata concept)	Foetus with hereditary disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2743034026) - 199531009 -> 303112003 (246454002) View
246454002 \|Occurrence (attribute)\|	303112003 \|Fetal period (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (328794028) - 199531009 -> 199516000 (116680003) View
116680003 \|Is a (attribute)\|	199516000 \|Known or suspected fetal abnormality (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (964907020) - 199531009 -> 55460000 (363698007) View
363698007 \|Finding site (attribute)\|	55460000 \|Fetal structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (964908026) - 199531009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4650730025) - 199531009 -> 32895009 (116680003) View
116680003 \|Is a (attribute)\|	32895009 \|Hereditary disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4650731026) - 199531009 -> 70591005 (116680003) View
116680003 \|Is a (attribute)\|	70591005 \|Fetal disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (964906027) - 199531009 -> 303112003 (246454002) View
246454002 \|Occurrence (attribute)\|	303112003 \|Fetal period (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
32895009 View
32895009	Hereditary disease (disorder)	Genetic disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
70591005 View
70591005	Fetal disorder (disorder)	Fetal disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1300190004 View
1300190004	Congenital pontocerebellar hypoplasia type 12 (disorder)	Pch12 - pontocerebellar hypoplasia type 12	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1237342004 View
1237342004	Lethal fetal cerebrorenogenitourinary agenesis or hypoplasia syndrome (disorder)	Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1220575002 View
1220575002	Fetal encasement syndrome (disorder)	Cocoon syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
725052002 View
725052002	Fetal cystic fibrosis (disorder)	Xơ nang bào thai	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
721232000 View
721232000	Hydrolethalus syndrome (disorder)	Hydrolethalus syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
700107006 View
700107006	Bartter syndrome antenatal type 1 (disorder)	Bartter's syndrome type 1	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
700109009 View
700109009	Bartter syndrome antenatal type 2 (disorder)	Bartter's syndrome type 2	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
5300004 View
5300004	Hemoglobin bart's hydrops syndrome (disorder)	Alpha thalassemia major	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 (c0619cd0-dee8-5b57-80ff-7d27c3d0bdfa) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	O35.2	TRUE	ALWAYS O35.2	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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