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Terminology chevron_right Concepts chevron_right 2109003

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Component

2109003

The component that hold information about this concept.

Fully Specified Name (FSN)

Isolated somatotropin deficiency (disorder)

Shortest Term

Isolated somatotropin deficiency

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

Isolated somatotropin deficiency (disorder)

SCTID: 2109003, Primitive, Active

2109003|Isolated somatotropin deficiency (disorder)|

en Isolated growth hormone deficiency
en Isolated growth hormone insufficiency
en Isolated somatotropin deficiency
en Isolated somatotropin deficiency (disorder)
en Ighd - isolated growth hormone deficiency

Expression

2109003 |Isolated somatotropin deficiency (disorder)|
 <<< 397827003 |Growth hormone deficiency (disorder)| : 
        { 363698007 |Finding site (attribute)| = 52618001 |Structure of pars distalis of pituitary (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
4651014 - Isolated growth hormone deficiency (en) View
4651014	en	Synonym (core metadata concept)	Isolated growth hormone deficiency	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
480919011 - Isolated growth hormone insufficiency (en) View
480919011	en	Synonym (core metadata concept)	Isolated growth hormone insufficiency	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
4650010 - Isolated somatotropin deficiency (en) View
4650010	en	Synonym (core metadata concept)	Isolated somatotropin deficiency	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
750346010 - Isolated somatotropin deficiency (disorder) (en) View
750346010	en	Fully specified name (core metadata concept)	Isolated somatotropin deficiency (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
480920017 - IGHD - Isolated growth hormone deficiency (en) View
480920017	en	Synonym (core metadata concept)	IGHD - Isolated growth hormone deficiency	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (3037978027) - 2109003 -> 52618001 (363698007) View
363698007 \|Finding site (attribute)\|	52618001 \|Structure of pars distalis of pituitary (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (182488024) - 2109003 -> 44008002 (116680003) View
116680003 \|Is a (attribute)\|	44008002 \|Somatotropin deficiency (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (725079026) - 2109003 -> 245533002 (363698007) View
363698007 \|Finding site (attribute)\|	245533002 \|Pars anterior of pituitary gland (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (182487025) - 2109003 -> 302867007 (116680003) View
116680003 \|Is a (attribute)\|	302867007 \|Growth hormone deficiency (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2225919024) - 2109003 -> 397827003 (116680003) View
116680003 \|Is a (attribute)\|	397827003 \|Growth hormone deficiency (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (725078023) - 2109003 -> 47563007 (363714003) View
363714003 \|Interprets (attribute)\|	47563007 \|Nutritional deficiency (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (725080028) - 2109003 -> 127944005 (363698007) View
363698007 \|Finding site (attribute)\|	127944005 \|Entire endocrine gonad (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
397827003 View
397827003	Growth hormone deficiency (disorder)	Thiếu hormon tăng trưởng	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
7990002 View
7990002	Immunoglobulinemia with isolated somatotropin deficiency (disorder)	Fleischer syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
18200000 View
18200000	Autosomal recessive isolated somatotropin deficiency (disorder)	Pituitary dwarfism type i	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
38576000 View
38576000	Nonfamilial hyperinsulinemic isolated somatotropin deficiency (disorder)	Ateliotic dwarfism with hyperinsulinemia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
237687003 View
237687003	Isolated growth hormone deficiency - autosomal dominant (disorder)	Autosomal dominant isolated somatotropin deficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (48e5e6a9-1c1b-5d19-9f09-0b12f93edade) 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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