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Terminology chevron_right Concepts chevron_right 128096008

Production

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Component

128096008

The component that hold information about this concept.

Fully Specified Name (FSN)

Hereditary platelet function disorder (disorder)

Shortest Term

Hereditary platelet function disorder

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

Hereditary platelet function disorder (disorder)

SCTID: 128096008, Primitive, Active

128096008|Hereditary platelet function disorder (disorder)|

en Hereditary platelet function disorder
en Hereditary platelet function disorder (disorder)

Expression

128096008 |Hereditary platelet function disorder (disorder)|
 <<< 234469001 |Inherited platelet disorder (disorder)| + 
267532001 |Qualitative platelet disorder (disorder)| : 
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
363714003 |Interprets (attribute)| = 74848003 |Hemostatic function (observable entity)| }
        { 363698007 |Finding site (attribute)| = 91689009 |Body system structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
194690019 - Hereditary platelet function disorder (en) View
194690019	en	Synonym (core metadata concept)	Hereditary platelet function disorder	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
732056019 - Hereditary platelet function disorder (disorder) (en) View
732056019	en	Fully specified name (core metadata concept)	Hereditary platelet function disorder (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (4785685025) - 128096008 -> 91689009 (363698007) View
363698007 \|Finding site (attribute)\|	91689009 \|Body system structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11290511026) - 128096008 -> 74848003 (363714003) View
363714003 \|Interprets (attribute)\|	74848003 \|Hemostatic function (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11290512022) - 128096008 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (163121020) - 128096008 -> 30577005 (116680003) View
116680003 \|Is a (attribute)\|	30577005 \|Qualitative platelet disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (696879025) - 128096008 -> 16378004 (363698007) View
363698007 \|Finding site (attribute)\|	16378004 \|Platelet (cell structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2728420025) - 128096008 -> 250311007 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	250311007 \|Platelet finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2785827027) - 128096008 -> 128153000 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	128153000 \|Hemostatic system finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3500197020) - 128096008 -> 267532001 (116680003) View
116680003 \|Is a (attribute)\|	267532001 \|Qualitative platelet disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (163120021) - 128096008 -> 363136009 (116680003) View
116680003 \|Is a (attribute)\|	363136009 \|Hereditary disorder of hematologic system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2264147028) - 128096008 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (696878022) - 128096008 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (163119026) - 128096008 -> 234469001 (116680003) View
116680003 \|Is a (attribute)\|	234469001 \|Inherited platelet disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
234469001 View
234469001	Inherited platelet disorder (disorder)	Hereditary thrombocytopathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
267532001 View
267532001	Qualitative platelet disorder (disorder)	Qualitative platelet defect	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1187614006 View
1187614006	Severe autosomal recessive macrothrombocytopenia (disorder)	Severe autosomal recessive macrothrombocytopenia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1172901009 View
1172901009	Cytosolic phospholipase-a2 alpha deficiency associated bleeding disorder (disorder)	Pla2g4a-related platelet dysfunction	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
782934004 View
782934004	Bleeding diathesis due to collagen receptor defect (disorder)	Bleeding diathesis due to collagen receptor defect	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
725105006 View
725105006	Bleeding disorder due to deficiency of calcium and diacylglycerol-regulated guanine nucleotide exchange factor i (disorder)	Bleeding disorder due to calcium and dag-regulated guanine exchange factor-1 deficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
725291001 View
725291001	Defect of purinergic receptor p2y g protein-coupled 12 (disorder)	P2y12 defect	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
32942005 View
32942005	Glanzmann's thrombasthenia (disorder)	Thrombasthenia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
43346008 View
43346008	Platelet procoagulant activity deficiency (disorder)	Platelet procoagulant activity deficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
51448009 View
51448009	Platelet secretory disorder (disorder)	Platelet secretory disorder	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
54569005 View
54569005	Bernard soulier syndrome (disorder)	Bernard-soulier syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
128098009 View
128098009	Scott syndrome (disorder)	Scott syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
128099001 View
128099001	Platelet storage pool defect (disorder)	Platelet storage pool defect	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
128102001 View
128102001	Familial alpha>2< adrenergic receptor defect in platelets (disorder)	Familial alpha>2< adrenergic receptor defect in platelets	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
128103006 View
128103006	Isolated collagen aggregation defect (disorder)	Isolated collagen aggregation defect	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
128115005 View
128115005	Pseudo von willebrand disease (disorder)	Pseudo von willebrand disease	900000000000074008 \|Necessary but not sufficient concept 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 (2851f505-98b4-533f-ae64-27a613dfe4a8) 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)\|
ExtendedMap object (c2c22b6e-5fcc-59ee-9958-2d9c7355aa28) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q89.9	TRUE	ALWAYS Q89.9	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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