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Terminology chevron_right Concepts chevron_right 237839005

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Component

237839005

The component that hold information about this concept.

Fully Specified Name (FSN)

Growth hormone receptor abnormality (disorder)

Shortest Term

Growth hormone receptor abnormality

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

Growth hormone receptor abnormality (disorder)

SCTID: 237839005, Primitive, Active

237839005|Growth hormone receptor abnormality (disorder)|

en Growth hormone receptor abnormality
en Growth hormone receptor abnormality (disorder)

Expression

237839005 |Growth hormone receptor abnormality (disorder)|
 <<< 38196001 |Laron-type isolated somatotropin defect (disorder)| : 
        { 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
356427012 - Growth hormone receptor abnormality (en) View
356427012	en	Synonym (core metadata concept)	Growth hormone receptor abnormality	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
626624016 - Growth hormone receptor abnormality (disorder) (en) View
626624016	en	Fully specified name (core metadata concept)	Growth hormone receptor abnormality (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (13280440026) - 237839005 -> 271603002 (363714003) View
363714003 \|Interprets (attribute)\|	271603002 \|Height / growth measure (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11572964028) - 237839005 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (526672026) - 237839005 -> 43451003 (116676008) View
116676008 \|Associated morphology (attribute)\|	43451003 \|Congenital deficiency (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2254096023) - 237839005 -> 62818001 (363698007) View
363698007 \|Finding site (attribute)\|	62818001 \|Adenohypophysis structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2575216027) - 237839005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (526674025) - 237839005 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (526676028) - 237839005 -> 245533002 (363698007) View
363698007 \|Finding site (attribute)\|	245533002 \|Pars anterior of pituitary gland (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (526673020) - 237839005 -> 47563007 (363714003) View
363714003 \|Interprets (attribute)\|	47563007 \|Nutritional deficiency (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (526675029) - 237839005 -> 127944005 (363698007) View
363698007 \|Finding site (attribute)\|	127944005 \|Entire endocrine gonad (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (53447020) - 237839005 -> 38196001 (116680003) View
116680003 \|Is a (attribute)\|	38196001 \|Laron-type isolated somatotropin defect (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
38196001 View
38196001	Laron-type isolated somatotropin defect (disorder)	Laron 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 (03d6161f-9640-5dd9-aa09-85e17514a041) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E34.8	TRUE	ALWAYS E34.8	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 (e6d33eaa-7b1a-50c2-93e3-d976410eedda) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E23.0	TRUE	ALWAYS E23.0	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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