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Terminology chevron_right Concepts chevron_right 778027003

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Component

778027003

The component that hold information about this concept.

Fully Specified Name (FSN)

Primary cd59 deficiency (disorder)

Shortest Term

Primary cd59 deficiency

Definition Status

900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Primary cd59 deficiency (disorder)

SCTID: 778027003, Primitive, Active

778027003|Primary cd59 deficiency (disorder)|

en Primary cd59 deficiency
en Primary cd59 deficiency (disorder)

Expression

778027003 |Primary cd59 deficiency (disorder)|
 <<< 234618008 |Complement regulatory factor defect (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
363138005 |Hereditary disorder of immune system (disorder)| + 
363235000 |Hereditary disorder of nervous system (disorder)| + 
12189000 |Coombs negative hemolytic anemia (disorder)| + 
414394009 |Hereditary red blood cell disorder (disorder)| + 
302226006 |Peripheral nerve disease (disorder)| + 
165397008 |Hemoglobin below reference range (finding)| : 
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 14089001 |Red blood cell count (procedure)| }
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 441689006 |Measurement of total hemoglobin concentration (procedure)| }
        { 363713009 |Has interpretation (attribute)| = 52101004 |Present (qualifier value)|,
363714003 |Interprets (attribute)| = 404227002 |Hemolysis (observable entity)| }
        { 363698007 |Finding site (attribute)| = 41898006 |Erythrocyte (cell)| }
        { 363698007 |Finding site (attribute)| = 84782009 |Peripheral nerve structure (body structure)| }
        { 370135005 |Pathological process (attribute)| = 769247005 |Abnormal immune process (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 116003000 |Structure of immune system (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3737312013 - Primary CD59 deficiency (en) View
3737312013	en	Synonym (core metadata concept)	Primary CD59 deficiency	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
3737313015 - Primary CD59 deficiency (disorder) (en) View
3737313015	en	Fully specified name (core metadata concept)	Primary CD59 deficiency (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13902508029) - 778027003 -> 165397008 (116680003) View
116680003 \|Is a (attribute)\|	165397008 \|Hemoglobin below reference range (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10725724020) - 778027003 -> 84782009 (363698007) View
363698007 \|Finding site (attribute)\|	84782009 \|Peripheral nerve structure (body structure)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10725727029) - 778027003 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10725728023) - 778027003 -> 116003000 (363698007) View
363698007 \|Finding site (attribute)\|	116003000 \|Structure of immune system (body structure)\|	7	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11171456020) - 778027003 -> 769247005 (370135005) View
370135005 \|Pathological process (attribute)\|	769247005 \|Abnormal immune process (qualifier value)\|	6	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10725714028) - 778027003 -> 234618008 (116680003) View
116680003 \|Is a (attribute)\|	234618008 \|Complement regulatory factor defect (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10725716026) - 778027003 -> 441689006 (363714003) View
363714003 \|Interprets (attribute)\|	441689006 \|Measurement of total hemoglobin concentration (procedure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10725717024) - 778027003 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10725718025) - 778027003 -> 363138005 (116680003) View
116680003 \|Is a (attribute)\|	363138005 \|Hereditary disorder of immune system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10725719022) - 778027003 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10725720027) - 778027003 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10725721028) - 778027003 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10725722024) - 778027003 -> 12189000 (116680003) View
116680003 \|Is a (attribute)\|	12189000 \|Coombs negative hemolytic anemia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10725723025) - 778027003 -> 414394009 (116680003) View
116680003 \|Is a (attribute)\|	414394009 \|Hereditary red blood cell disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10725725021) - 778027003 -> 302226006 (116680003) View
116680003 \|Is a (attribute)\|	302226006 \|Peripheral nerve disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10725726022) - 778027003 -> 14089001 (363714003) View
363714003 \|Interprets (attribute)\|	14089001 \|Red blood cell count (procedure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11105645029) - 778027003 -> 404227002 (363714003) View
363714003 \|Interprets (attribute)\|	404227002 \|Hemolysis (observable entity)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11105646028) - 778027003 -> 52101004 (363713009) View
363713009 \|Has interpretation (attribute)\|	52101004 \|Present (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
302226006 View
302226006	Peripheral nerve disease (disorder)	Peripheral neuropathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
165397008 View
165397008	Hemoglobin below reference range (finding)	Hemoglobin low	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
414394009 View
414394009	Hereditary red blood cell disorder (disorder)	Hereditary red blood cell disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
12189000 View
12189000	Coombs negative hemolytic anemia (disorder)	Coombs negative hemolytic anemia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
85995004 View
85995004	Autosomal recessive hereditary disorder (disorder)	Hereditary disorder trait, nos	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
234618008 View
234618008	Complement regulatory factor defect (disorder)	Complement regulatory factor defect	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363138005 View
363138005	Hereditary disorder of immune system (disorder)	Hereditary disorder of immune system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363235000 View
363235000	Hereditary disorder of nervous system (disorder)	Hereditary disorder of nervous system	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 (f9a868ee-14c6-5c82-83ac-31b8af0cb782) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D84.1	TRUE	ALWAYS D84.1 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION	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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