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Terminology chevron_right Concepts chevron_right 32942005

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Component

32942005

The component that hold information about this concept.

Fully Specified Name (FSN)

Glanzmann's thrombasthenia (disorder)

Shortest Term

Thrombasthenia

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

Glanzmann's thrombasthenia (disorder)

SCTID: 32942005, Primitive, Active

32942005|Glanzmann's thrombasthenia (disorder)|

en Hereditary haemorrhagic thrombasthenia
en Hereditary hemorrhagic thrombasthenia
en Hereditary thromboasthenia
en Thrombasthenia
en Glanzmann's disease
en Glanzmann's syndrome
en Glanzmann's thrombasthenia (disorder)
en Glanzmann-naegeli disorder
en Glanzmann's thrombasthenia
en Glanzmann thromboasthenia

Expression

32942005 |Glanzmann's thrombasthenia (disorder)|
 <<< 234470000 |Platelet membrane defect (disorder)| + 
128096008 |Hereditary platelet function disorder (disorder)| : 
        { 363698007 |Finding site (attribute)| = 91689009 |Body system structure (body structure)| }
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
363714003 |Interprets (attribute)| = 74848003 |Hemostatic function (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
1216410012 - Hereditary haemorrhagic thrombasthenia (en) View
1216410012	en	Synonym (core metadata concept)	Hereditary haemorrhagic thrombasthenia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
1217904013 - Hereditary hemorrhagic thrombasthenia (en) View
1217904013	en	Synonym (core metadata concept)	Hereditary hemorrhagic thrombasthenia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
54984011 - Hereditary thromboasthenia (en) View
54984011	en	Synonym (core metadata concept)	Hereditary thromboasthenia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
54989018 - Thrombasthenia (en) View
54989018	en	Synonym (core metadata concept)	Thrombasthenia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
2646881012 - Glanzmann's disease (en) View
2646881012	en	Synonym (core metadata concept)	Glanzmann's disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
1228016018 - Glanzsmann's disease (en) View
1228016018	en	Synonym (core metadata concept)	Glanzsmann's disease	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
1228017010 - Glanzmann's syndrome (en) View
1228017010	en	Synonym (core metadata concept)	Glanzmann's syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
764285014 - Glanzmann's thrombasthenia (disorder) (en) View
764285014	en	Fully specified name (core metadata concept)	Glanzmann's thrombasthenia (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
54987016 - Glanzmann-Naegeli disorder (en) View
54987016	en	Synonym (core metadata concept)	Glanzmann-Naegeli disorder	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
196971014 - Glanzmann's thrombasthenia (en) View
196971014	en	Synonym (core metadata concept)	Glanzmann's thrombasthenia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
54986013 - Glanzmann thromboasthenia (en) View
54986013	en	Synonym (core metadata concept)	Glanzmann thromboasthenia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
54985012 - Hereditary thromboasthenia, NOS (en) View
54985012	en	Synonym (core metadata concept)	Hereditary thromboasthenia, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
54988014 - Thrombasthenia, NOS (en) View
54988014	en	Synonym (core metadata concept)	Thrombasthenia, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (4784651022) - 32942005 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12436769029) - 32942005 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11572522020) - 32942005 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11572523026) - 32942005 -> 74848003 (363714003) View
363714003 \|Interprets (attribute)\|	74848003 \|Hemostatic function (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (754217020) - 32942005 -> 16378004 (363698007) View
363698007 \|Finding site (attribute)\|	16378004 \|Platelet (cell structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2731336028) - 32942005 -> 250311007 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	250311007 \|Platelet finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2786801022) - 32942005 -> 128153000 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	128153000 \|Hemostatic system finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2266073022) - 32942005 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (754216027) - 32942005 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (201584021) - 32942005 -> 234470000 (116680003) View
116680003 \|Is a (attribute)\|	234470000 \|Platelet membrane defect (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (201585022) - 32942005 -> 128096008 (116680003) View
116680003 \|Is a (attribute)\|	128096008 \|Hereditary platelet function disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
128096008 View
128096008	Hereditary platelet function disorder (disorder)	Hereditary platelet function disorder	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
234470000 View
234470000	Platelet membrane defect (disorder)	Platelet membrane defect	900000000000074008 \|Necessary but not sufficient concept 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 (9448a145-3cf7-51d2-9660-8126d8c8b66c) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D69.1	TRUE	ALWAYS D69.1	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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