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Terminology chevron_right Concepts chevron_right 715526002

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Component

715526002

The component that hold information about this concept.

Fully Specified Name (FSN)

Dehydrated hereditary stomatocytosis (disorder)

Shortest Term

Hereditary xerocytosis

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

Dehydrated hereditary stomatocytosis (disorder)

SCTID: 715526002, Primitive, Active

715526002|Dehydrated hereditary stomatocytosis (disorder)|

en Dehydrated hereditary stomatocytosis
en Dehydrated hereditary stomatocytosis (disorder)
en Hereditary xerocytosis

Expression

715526002 |Dehydrated hereditary stomatocytosis (disorder)|
 <<< 11164009 |Autosomal dominant hereditary disorder (disorder)| + 
3272007 |Stomatocytosis (disorder)| + 
414394009 |Hereditary red blood cell disorder (disorder)| + 
111575000 |Anemia due to membrane defect (disorder)| + 
234401000 |Erythrocyte enzyme deficiency (disorder)| : 
        { 363713009 |Has interpretation (attribute)| = 52101004 |Present (qualifier value)|,
363714003 |Interprets (attribute)| = 404227002 |Hemolysis (observable entity)| }
        { 363713009 |Has interpretation (attribute)| = 281300000 |Below reference range (qualifier value)|,
363714003 |Interprets (attribute)| = 14089001 |Red blood cell count (procedure)| }
        { 116676008 |Associated morphology (attribute)| = 10636005 |Stomatocyte (cell)| }
        { 363698007 |Finding site (attribute)| = 41898006 |Erythrocyte (cell)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3302920015 - Dehydrated hereditary stomatocytosis (en) View
3302920015	en	Synonym (core metadata concept)	Dehydrated hereditary stomatocytosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3302919014 - Dehydrated hereditary stomatocytosis (disorder) (en) View
3302919014	en	Fully specified name (core metadata concept)	Dehydrated hereditary stomatocytosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3302921016 - Hereditary xerocytosis (en) View
3302921016	en	Synonym (core metadata concept)	Hereditary xerocytosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6765419027) - 715526002 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16363054028) - 715526002 -> 111575000 (116680003) View
116680003 \|Is a (attribute)\|	111575000 \|Anemia due to membrane defect (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16363055027) - 715526002 -> 404227002 (363714003) View
363714003 \|Interprets (attribute)\|	404227002 \|Hemolysis (observable entity)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16363056026) - 715526002 -> 52101004 (363713009) View
363713009 \|Has interpretation (attribute)\|	52101004 \|Present (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16363057024) - 715526002 -> 14089001 (363714003) View
363714003 \|Interprets (attribute)\|	14089001 \|Red blood cell count (procedure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6547021024) - 715526002 -> 14087004 (116680003) View
116680003 \|Is a (attribute)\|	14087004 \|Hereditary stomatocytosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6765417025) - 715526002 -> 281300000 (363713009) View
363713009 \|Has interpretation (attribute)\|	281300000 \|Below reference range (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6765418024) - 715526002 -> 14089001 (363714003) View
363714003 \|Interprets (attribute)\|	14089001 \|Red blood cell count (procedure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6765420022) - 715526002 -> 441689006 (363714003) View
363714003 \|Interprets (attribute)\|	441689006 \|Measurement of total hemoglobin concentration (procedure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13891304029) - 715526002 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13891305028) - 715526002 -> 234401000 (116680003) View
116680003 \|Is a (attribute)\|	234401000 \|Erythrocyte enzyme deficiency (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13891306027) - 715526002 -> 3272007 (116680003) View
116680003 \|Is a (attribute)\|	3272007 \|Stomatocytosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13891307020) - 715526002 -> 414394009 (116680003) View
116680003 \|Is a (attribute)\|	414394009 \|Hereditary red blood cell disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6547020020) - 715526002 -> 10636005 (116676008) View
116676008 \|Associated morphology (attribute)\|	10636005 \|Stomatocyte (cell)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6547022028) - 715526002 -> 41898006 (363698007) View
363698007 \|Finding site (attribute)\|	41898006 \|Erythrocyte (cell)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6547023022) - 715526002 -> 62574001 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	62574001 \|Erythropenia (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
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
3272007 View
3272007	Stomatocytosis (disorder)	Stomatocytosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
111575000 View
111575000	Anemia due to membrane defect (disorder)	Anemia due to membrane defect	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
234401000 View
234401000	Erythrocyte enzyme deficiency (disorder)	Erythrocyte enzyme deficiency	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 (89e4698b-09b6-5020-bcd4-445739966969) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D58.8	TRUE	ALWAYS D58.8 \| 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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