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Terminology chevron_right Concepts chevron_right 700102000

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Component

700102000

The component that hold information about this concept.

Fully Specified Name (FSN)

Hereditary disease suspected (situation)

Shortest Term

Hereditary disease suspected

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

Hereditary disease suspected (situation)

SCTID: 700102000, Defined, Active

700102000|Hereditary disease suspected (situation)|

en Hereditary disease suspected
en Hereditary disease suspected (situation)

Expression

700102000 |Hereditary disease suspected (situation)|
 === 41769001 |Disease suspected (situation)| : 
        { 246090004 |Associated finding (attribute)| = 32895009 |Hereditary disease (disorder)|,
408729009 |Finding context (attribute)| = 415684004 |Suspected (qualifier value)|,
408732007 |Subject relationship context (attribute)| = 410604004 |Subject of record (person)|,
408731000 |Temporal context (attribute)| = 410512000 |Current or specified time (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
5438489015 - Hereditary disease suspected (en) View
5438489015	en	Synonym (core metadata concept)	Hereditary disease suspected	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
5438488011 - Hereditary disease suspected (situation) (en) View
5438488011	en	Fully specified name (core metadata concept)	Hereditary disease suspected (situation)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2989388010 - Suspected hereditary disease (en) View
2989388010	en	Synonym (core metadata concept)	Suspected hereditary disease	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	False
2989498015 - Suspected hereditary disease (situation) (en) View
2989498015	en	Fully specified name (core metadata concept)	Suspected hereditary disease (situation)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (4952575022) - 700102000 -> 41769001 (116680003) View
116680003 \|Is a (attribute)\|	41769001 \|Disease suspected (situation)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4952576023) - 700102000 -> 32895009 (246090004) View
246090004 \|Associated finding (attribute)\|	32895009 \|Hereditary disease (disorder)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4952577025) - 700102000 -> 410604004 (408732007) View
408732007 \|Subject relationship context (attribute)\|	410604004 \|Subject of record (person)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4952578024) - 700102000 -> 410512000 (408731000) View
408731000 \|Temporal context (attribute)\|	410512000 \|Current or specified time (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4952579027) - 700102000 -> 415684004 (408729009) View
408729009 \|Finding context (attribute)\|	415684004 \|Suspected (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
41769001 View
41769001	Disease suspected (situation)	Disease suspected	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1356827009 View
1356827009	Fetal hereditary disease suspected (situation)	Fetal hereditary disease suspected	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
473131004 View
473131004	Sickle cell disease suspected (situation)	Sickle cell disease suspected	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
428301001 View
428301001	Cystic fibrosis suspected (situation)	Cystic fibrosis suspected	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
428485006 View
428485006	Sickle cell trait suspected (situation)	Sickle cell trait suspected	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
428655008 View
428655008	Phenylketonuria suspected (situation)	Phenylketonuria suspected	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
429244009 View
429244009	Medium-chain acyl-coenzyme a dehydrogenase deficiency suspected (situation)	Medium-chain acyl-coenzyme a dehydrogenase deficiency suspected	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 (975fabec-ccf0-5bfb-9621-dbdd3896746b) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|

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