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Terminology chevron_right Concepts chevron_right 15069006

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Component

15069006

The component that hold information about this concept.

Fully Specified Name (FSN)

Russell-silver syndrome (disorder)

Shortest Term

Silver 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

Russell-silver syndrome (disorder)

SCTID: 15069006, Primitive, Active

15069006|Russell-silver syndrome (disorder)|

en Silver syndrome
en Russell-silver syndrome (disorder)
en Russell-silver syndrome
en Russell's syndrome

Expression

15069006 |Russell-silver syndrome (disorder)|
 <<< 41483000 |Multiple malformation syndrome, small stature, without skeletal dysplasia (disorder)| + 
237837007 |Primordial dwarfism (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363714003 |Interprets (attribute)| = 271603002 |Height / growth measure (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
25587016 - Silver syndrome (en) View
25587016	en	Synonym (core metadata concept)	Silver syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
741719019 - Russell-Silver syndrome (disorder) (en) View
741719019	en	Fully specified name (core metadata concept)	Russell-Silver syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
25586013 - Russell-Silver syndrome (en) View
25586013	en	Synonym (core metadata concept)	Russell-Silver syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
25588014 - Russell's syndrome (en) View
25588014	en	Synonym (core metadata concept)	Russell's syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13280379020) - 15069006 -> 271603002 (363714003) View
363714003 \|Interprets (attribute)\|	271603002 \|Height / growth measure (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5019701029) - 15069006 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10528627024) - 15069006 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10528628025) - 15069006 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (706637020) - 15069006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2264467025) - 15069006 -> 112635002 (116676008) View
116676008 \|Associated morphology (attribute)\|	112635002 \|Congenital malformation (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4995242026) - 15069006 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3282782028) - 15069006 -> 237837007 (116680003) View
116680003 \|Is a (attribute)\|	237837007 \|Primordial dwarfism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (170428021) - 15069006 -> 312573007 (116680003) View
116680003 \|Is a (attribute)\|	312573007 \|Multisystem disorder q-r (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (170429029) - 15069006 -> 41483000 (116680003) View
116680003 \|Is a (attribute)\|	41483000 \|Multiple malformation syndrome, small stature, without skeletal dysplasia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
41483000 View
41483000	Multiple malformation syndrome, small stature, without skeletal dysplasia (disorder)	Multiple malformation syndrome, small stature, without skeletal dysplasia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
237837007 View
237837007	Primordial dwarfism (disorder)	Nanosoma	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 (6856b249-530f-5b6e-97a0-54993059e2da) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q87.1	TRUE	ALWAYS Q87.1	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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