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Terminology chevron_right Concepts chevron_right 1172901009

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Component

1172901009

The component that hold information about this concept.

Fully Specified Name (FSN)

Cytosolic phospholipase-a2 alpha deficiency associated bleeding disorder (disorder)

Shortest Term

Pla2g4a-related platelet dysfunction

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

Cytosolic phospholipase-a2 alpha deficiency associated bleeding disorder (disorder)

SCTID: 1172901009, Primitive, Active

1172901009|Cytosolic phospholipase-a2 alpha deficiency associated bleeding disorder (disorder)|

en Cytosolic phospholipase-a2 alpha deficiency associated bleeding disorder
en Cytosolic phospholipase-a2 alpha deficiency associated bleeding disorder (disorder)
en Pla2g4a (phospholipase a2 group iva) related platelet dysfunction
en Pla2g4a-related platelet dysfunction
en Platelet dysfunction due to cytosolic phospholipase-a2 alpha deficiency

Expression

1172901009 |Cytosolic phospholipase-a2 alpha deficiency associated bleeding disorder (disorder)|
 <<< 128096008 |Hereditary platelet function disorder (disorder)| + 
363080007 |Digestive system hereditary disorder (disorder)| + 
85995004 |Autosomal recessive hereditary disorder (disorder)| + 
40845000 |Gastrointestinal ulcer (disorder)| + 
58184002 |Recurrent disease (disorder)| : 
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
363714003 |Interprets (attribute)| = 74848003 |Hemostatic function (observable entity)| }
        { 116676008 |Associated morphology (attribute)| = 56208002 |Ulcer (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 122865005 |Gastrointestinal tract structure (body structure)| }
        { 263502005 |Clinical course (attribute)| = 255227004 |Recurrent (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
4636409011 - Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (en) View
4636409011	en	Synonym (core metadata concept)	Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
4636405017 - Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) (en) View
4636405017	en	Fully specified name (core metadata concept)	Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
4636406016 - PLA2G4A (phospholipase A2 group IVA) related platelet dysfunction (en) View
4636406016	en	Synonym (core metadata concept)	PLA2G4A (phospholipase A2 group IVA) related platelet dysfunction	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
4636407013 - PLA2G4A-related platelet dysfunction (en) View
4636407013	en	Synonym (core metadata concept)	PLA2G4A-related platelet dysfunction	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
4636408015 - Platelet dysfunction due to cytosolic phospholipase-A2 alpha deficiency (en) View
4636408015	en	Synonym (core metadata concept)	Platelet dysfunction due to cytosolic phospholipase-A2 alpha deficiency	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (14020812028) - 1172901009 -> 128284006 (116680003) View
116680003 \|Is a (attribute)\|	128284006 \|Chronic digestive system disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14020817023) - 1172901009 -> 42433008 (116676008) View
116676008 \|Associated morphology (attribute)\|	42433008 \|Recurrent ulcer (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15147216020) - 1172901009 -> 56208002 (116676008) View
116676008 \|Associated morphology (attribute)\|	56208002 \|Ulcer (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14020805021) - 1172901009 -> 128096008 (116680003) View
116680003 \|Is a (attribute)\|	128096008 \|Hereditary platelet function disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14020806022) - 1172901009 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14020808023) - 1172901009 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14020810020) - 1172901009 -> 74848003 (363714003) View
363714003 \|Interprets (attribute)\|	74848003 \|Hemostatic function (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14020811024) - 1172901009 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14020813022) - 1172901009 -> 40845000 (116680003) View
116680003 \|Is a (attribute)\|	40845000 \|Gastrointestinal ulcer (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14020814027) - 1172901009 -> 58184002 (116680003) View
116680003 \|Is a (attribute)\|	58184002 \|Recurrent disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14020815026) - 1172901009 -> 255227004 (263502005) View
263502005 \|Clinical course (attribute)\|	255227004 \|Recurrent (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14020816025) - 1172901009 -> 122865005 (363698007) View
363698007 \|Finding site (attribute)\|	122865005 \|Gastrointestinal tract structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
58184002 View
58184002	Recurrent disease (disorder)	Recurrent disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
40845000 View
40845000	Gastrointestinal ulcer (disorder)	Gastrointestinal ulcer	900000000000073002 \|Sufficiently defined by necessary conditions 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
128096008 View
128096008	Hereditary platelet function disorder (disorder)	Hereditary platelet function disorder	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363080007 View
363080007	Digestive system hereditary disorder (disorder)	Digestive system hereditary disorder	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 (2fdc6219-0407-5c54-b650-ec7f6852b560) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D69.1	TRUE	ALWAYS D69.1 \| 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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