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Terminology chevron_right Concepts chevron_right 403837005

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Component

403837005

The component that hold information about this concept.

Fully Specified Name (FSN)

Wiskott-aldrich autosomal dominant variant syndrome (disorder)

Shortest Term

Wiskott-aldrich autosomal dominant variant syndrome

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

Wiskott-aldrich autosomal dominant variant syndrome (disorder)

SCTID: 403837005, Primitive, Active

403837005|Wiskott-aldrich autosomal dominant variant syndrome (disorder)|

en Wiskott-aldrich autosomal dominant variant syndrome
en Wiskott-aldrich autosomal dominant variant syndrome (disorder)

Expression

403837005 |Wiskott-aldrich autosomal dominant variant syndrome (disorder)|
 <<< 36070007 |Wiskott-aldrich syndrome (disorder)| : 
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 61928009 |Platelet count (procedure)| }
        { 363713009 |Has interpretation (attribute)| = 263654008 |Abnormal (qualifier value)|,
363714003 |Interprets (attribute)| = 74848003 |Hemostatic function (observable entity)| }
        { 363698007 |Finding site (attribute)| = 116003000 |Structure of immune system (body structure)| }
        { 246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 370135005 |Pathological process (attribute)| = 769247005 |Abnormal immune process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
1782841017 - Wiskott-Aldrich autosomal dominant variant syndrome (en) View
1782841017	en	Synonym (core metadata concept)	Wiskott-Aldrich autosomal dominant variant syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
1771763014 - Wiskott-Aldrich autosomal dominant variant syndrome (disorder) (en) View
1771763014	en	Fully specified name (core metadata concept)	Wiskott-Aldrich autosomal dominant variant syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2291266026) - 403837005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11170210020) - 403837005 -> 769247005 (370135005) View
370135005 \|Pathological process (attribute)\|	769247005 \|Abnormal immune process (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14976352024) - 403837005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (14976390029) - 403837005 -> 769247005 (370135005) View
370135005 \|Pathological process (attribute)\|	769247005 \|Abnormal immune process (qualifier value)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11289372021) - 403837005 -> 74848003 (363714003) View
363714003 \|Interprets (attribute)\|	74848003 \|Hemostatic function (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12436909021) - 403837005 -> 74848003 (363714003) View
363714003 \|Interprets (attribute)\|	74848003 \|Hemostatic function (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2291272026) - 403837005 -> 116003000 (363698007) View
363698007 \|Finding site (attribute)\|	116003000 \|Structure of immune system (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11289373027) - 403837005 -> 263654008 (363713009) View
363713009 \|Has interpretation (attribute)\|	263654008 \|Abnormal (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2755637025) - 403837005 -> 106182000 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	106182000 \|Immune system finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4779230023) - 403837005 -> 415116008 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	415116008 \|Platelet count below reference range (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6787469028) - 403837005 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6787470027) - 403837005 -> 61928009 (363714003) View
363714003 \|Interprets (attribute)\|	61928009 \|Platelet count (procedure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2291267024) - 403837005 -> 16378004 (363698007) View
363698007 \|Finding site (attribute)\|	16378004 \|Platelet (cell structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2755638024) - 403837005 -> 415116008 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	415116008 \|Platelet count below reference range (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2798258020) - 403837005 -> 128153000 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	128153000 \|Hemostatic system finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3331310025) - 403837005 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3331311026) - 403837005 -> 23583003 (116676008) View
116676008 \|Associated morphology (attribute)\|	23583003 \|Inflammation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2291268025) - 403837005 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2291269022) - 403837005 -> 23583003 (116676008) View
116676008 \|Associated morphology (attribute)\|	23583003 \|Inflammation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2291270023) - 403837005 -> 4538007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4538007 \|Papulovesicular rash (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2291271022) - 403837005 -> 57171008 (363698007) View
363698007 \|Finding site (attribute)\|	57171008 \|Hematopoietic system structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2515346029) - 403837005 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2250523022) - 403837005 -> 36070007 (116680003) View
116680003 \|Is a (attribute)\|	36070007 \|Wiskott-aldrich syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
36070007 View
36070007	Wiskott-aldrich syndrome (disorder)	Aldrich syndrome	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 (d55a2b8f-6b48-52fe-8608-daca77c7a11f) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D82.0	TRUE	ALWAYS D82.0	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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