dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 715532007

Production

add

Component

715532007

The component that hold information about this concept.

Fully Specified Name (FSN)

Weismann netter syndrome (disorder)

Shortest Term

Weismann netter 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

Weismann netter syndrome (disorder)

SCTID: 715532007, Primitive, Active

715532007|Weismann netter syndrome (disorder)|

en Anterior bowing of legs with dwarfism
en Weismann netter syndrome
en Weismann netter syndrome (disorder)

Expression

715532007 |Weismann netter syndrome (disorder)|
 <<< 278832007 |Bent bone dysplasia group (disorder)| + 
782964007 |Genetic disease (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 25723000 |Dysplasia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 272673000 |Bone structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3302948015 - Anterior bowing of legs with dwarfism (en) View
3302948015	en	Synonym (core metadata concept)	Anterior bowing of legs with dwarfism	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3302947013 - Weismann Netter syndrome (en) View
3302947013	en	Synonym (core metadata concept)	Weismann Netter syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
3302945017 - Weismann Netter syndrome (disorder) (en) View
3302945017	en	Fully specified name (core metadata concept)	Weismann Netter syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15444611026) - 715532007 -> 782964007 (116680003) View
116680003 \|Is a (attribute)\|	782964007 \|Genetic disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10514155027) - 715532007 -> 25283002 (116676008) View
116676008 \|Associated morphology (attribute)\|	25283002 \|Congenital dysplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11226429024) - 715532007 -> 25723000 (116676008) View
116676008 \|Associated morphology (attribute)\|	25723000 \|Dysplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6547063023) - 715532007 -> 25283002 (116676008) View
116676008 \|Associated morphology (attribute)\|	25283002 \|Congenital dysplasia (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6547064028) - 715532007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6547065027) - 715532007 -> 272673000 (363698007) View
363698007 \|Finding site (attribute)\|	272673000 \|Bone structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10514153023) - 715532007 -> 272673000 (363698007) View
363698007 \|Finding site (attribute)\|	272673000 \|Bone structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10514154028) - 715532007 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10514156026) - 715532007 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6547062029) - 715532007 -> 278832007 (116680003) View
116680003 \|Is a (attribute)\|	278832007 \|Bent bone dysplasia group (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
782964007 View
782964007	Genetic disease (disorder)	Genetic disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
278832007 View
278832007	Bent bone dysplasia group (disorder)	Bent bone dysplasia group	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 (ed002d6f-d453-55ce-8b05-b1aff329c5fc) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q77.8	TRUE	ALWAYS Q77.8 \| 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)\|

Terminology chevron_right Concepts chevron_right 715532007

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches