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Terminology chevron_right Concepts chevron_right 718182008

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Component

718182008

The component that hold information about this concept.

Fully Specified Name (FSN)

Combined pituitary hormone deficiency genetic form (disorder)

Shortest Term

Familial congenital hypopituitarism

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

Combined pituitary hormone deficiency genetic form (disorder)

SCTID: 718182008, Primitive, Active

718182008|Combined pituitary hormone deficiency genetic form (disorder)|

en Combined pituitary hormone deficiency genetic form
en Combined pituitary hormone deficiency genetic form (disorder)
en Familial congenital hypopituitarism
en Multiple pituitary hormone deficiency genetic form

Expression

718182008 |Combined pituitary hormone deficiency genetic form (disorder)|
 <<< 66091009 |Congenital disease (disorder)| + 
74728003 |Hypopituitarism (disorder)| + 
363104002 |Hereditary disorder of endocrine system (disorder)| + 
363235000 |Hereditary disorder of nervous system (disorder)| : 
        { 363698007 |Finding site (attribute)| = 56329008 |Pituitary structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3311409015 - Combined pituitary hormone deficiency genetic form (en) View
3311409015	en	Synonym (core metadata concept)	Combined pituitary hormone deficiency genetic form	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3311175017 - Combined pituitary hormone deficiency genetic form (disorder) (en) View
3311175017	en	Fully specified name (core metadata concept)	Combined pituitary hormone deficiency genetic form (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3311172019 - Familial congenital hypopituitarism (en) View
3311172019	en	Synonym (core metadata concept)	Familial congenital hypopituitarism	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3311410013 - Multiple pituitary hormone deficiency genetic form (en) View
3311410013	en	Synonym (core metadata concept)	Multiple pituitary hormone deficiency genetic form	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6594949020) - 718182008 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594953022) - 718182008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6594954027) - 718182008 -> 56329008 (363698007) View
363698007 \|Finding site (attribute)\|	56329008 \|Pituitary structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7112380024) - 718182008 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (7112381023) - 718182008 -> 56329008 (363698007) View
363698007 \|Finding site (attribute)\|	56329008 \|Pituitary structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594950020) - 718182008 -> 74728003 (116680003) View
116680003 \|Is a (attribute)\|	74728003 \|Hypopituitarism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594951024) - 718182008 -> 363104002 (116680003) View
116680003 \|Is a (attribute)\|	363104002 \|Hereditary disorder of endocrine system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6594952028) - 718182008 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
66091009 View
66091009	Congenital disease (disorder)	Congenital disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
74728003 View
74728003	Hypopituitarism (disorder)	Hypopituitarism	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363104002 View
363104002	Hereditary disorder of endocrine system (disorder)	Hereditary disorder of endocrine system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
363235000 View
363235000	Hereditary disorder of nervous system (disorder)	Hereditary disorder of nervous system	900000000000073002 \|Sufficiently defined by necessary conditions 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 (47ad2f44-aaea-5ea9-980f-552fc16fdf81) 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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