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Terminology chevron_right Concepts chevron_right 716697002

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Component

716697002

The component that hold information about this concept.

Fully Specified Name (FSN)

Hereditary persistence of alpha-fetoprotein (disorder)

Shortest Term

Hereditary persistence of alpha-fetoprotein

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 persistence of alpha-fetoprotein (disorder)

SCTID: 716697002, Defined, Active

716697002|Hereditary persistence of alpha-fetoprotein (disorder)|

en Hereditary persistence of alpha-fetoprotein
en Hereditary persistence of alpha-fetoprotein (disorder)

Expression

716697002 |Hereditary persistence of alpha-fetoprotein (disorder)|
 === 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
27624003 |Chronic disease (disorder)| + 
166561008 |Alpha-fetoprotein above reference range (finding)| : 
        { 363713009 |Has interpretation (attribute)| = 281302008 |Above reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 80152001 |Alpha-1-fetoprotein measurement (procedure)| }
        { 263502005 |Clinical course (attribute)| = 62459000 |Chronic persistent (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3307235018 - Hereditary persistence of alpha-fetoprotein (en) View
3307235018	en	Synonym (core metadata concept)	Hereditary persistence of alpha-fetoprotein	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3307234019 - Hereditary persistence of alpha-fetoprotein (disorder) (en) View
3307234019	en	Fully specified name (core metadata concept)	Hereditary persistence of alpha-fetoprotein (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6594723020) - 716697002 -> 441772009 (116680003) View
116680003 \|Is a (attribute)\|	441772009 \|Abnormal presence of alpha-fetoprotein (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6594724025) - 716697002 -> 43261007 (363713009) View
363713009 \|Has interpretation (attribute)\|	43261007 \|Abnormal presence of (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13691277020) - 716697002 -> 27624003 (116680003) View
116680003 \|Is a (attribute)\|	27624003 \|Chronic disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13691278026) - 716697002 -> 166561008 (116680003) View
116680003 \|Is a (attribute)\|	166561008 \|Alpha-fetoprotein above reference range (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13691279023) - 716697002 -> 62459000 (263502005) View
263502005 \|Clinical course (attribute)\|	62459000 \|Chronic persistent (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13691280021) - 716697002 -> 281302008 (363713009) View
363713009 \|Has interpretation (attribute)\|	281302008 \|Above reference range (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594722026) - 716697002 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594725029) - 716697002 -> 80152001 (363714003) View
363714003 \|Interprets (attribute)\|	80152001 \|Alpha-1-fetoprotein measurement (procedure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
166561008 View
166561008	Alpha-fetoprotein above reference range (finding)	Alpha-fetoprotein raised	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
27624003 View
27624003	Chronic disease (disorder)	Chronic disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (031a14c5-b4e3-5f5b-9aea-319af89f8c90) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	R77.2	TRUE	ALWAYS R77.2	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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