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Terminology chevron_right Concepts chevron_right 773645004

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Component

773645004

The component that hold information about this concept.

Fully Specified Name (FSN)

Familial infantile gigantism (disorder)

Shortest Term

Familial infantile gigantism

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

Familial infantile gigantism (disorder)

SCTID: 773645004, Primitive, Active

773645004|Familial infantile gigantism (disorder)|

en Familial infantile gigantism
en Familial infantile gigantism (disorder)
en Hereditary infantile gigantism
en Infantile gigantism due to pituitary hyperplasia

Expression

773645004 |Familial infantile gigantism (disorder)|
 <<< 86073008 |Hypersomatotropic gigantism (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| + 
363104002 |Hereditary disorder of endocrine system (disorder)| + 
363235000 |Hereditary disorder of nervous system (disorder)| + 
1162984000 |X-linked dominant hereditary disease (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 48707006 |Growth acceleration (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 52618001 |Structure of pars distalis of pituitary (body structure)|,
246454002 |Occurrence (attribute)| = 3658006 |Infancy (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 35105006 |Increased (qualifier value)|,
363714003 |Interprets (attribute)| = 35188005 |Hormone production, function (observable entity)| }
        { 42752001 |Due to (attribute)| = 3652007 |Overproduction of growth hormone (disorder)| }
        { 363714003 |Interprets (attribute)| = 271603002 |Height / growth measure (observable entity)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3725354018 - Familial infantile gigantism (en) View
3725354018	en	Synonym (core metadata concept)	Familial infantile gigantism	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3725353012 - Familial infantile gigantism (disorder) (en) View
3725353012	en	Fully specified name (core metadata concept)	Familial infantile gigantism (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3725352019 - Hereditary infantile gigantism (en) View
3725352019	en	Synonym (core metadata concept)	Hereditary infantile gigantism	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3725356016 - Infantile gigantism due to pituitary hyperplasia (en) View
3725356016	en	Synonym (core metadata concept)	Infantile gigantism due to pituitary hyperplasia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (10624621026) - 773645004 -> 128430005 (116680003) View
116680003 \|Is a (attribute)\|	128430005 \|X-linked hereditary disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (14011007021) - 773645004 -> 1162984000 (116680003) View
116680003 \|Is a (attribute)\|	1162984000 \|X-linked dominant hereditary disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12876747023) - 773645004 -> 363104002 (116680003) View
116680003 \|Is a (attribute)\|	363104002 \|Hereditary disorder of endocrine system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13070003020) - 773645004 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13280645027) - 773645004 -> 271603002 (363714003) View
363714003 \|Interprets (attribute)\|	271603002 \|Height / growth measure (observable entity)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624618028) - 773645004 -> 83649006 (42752001) View
42752001 \|Due to (attribute)\|	83649006 \|Increased hormone secretion (finding)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11573410029) - 773645004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12095745023) - 773645004 -> 3652007 (42752001) View
42752001 \|Due to (attribute)\|	3652007 \|Overproduction of growth hormone (disorder)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12095746024) - 773645004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624615025) - 773645004 -> 35105006 (363713009) View
363713009 \|Has interpretation (attribute)\|	35105006 \|Increased (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624616029) - 773645004 -> 35188005 (363714003) View
363714003 \|Interprets (attribute)\|	35188005 \|Hormone production, function (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624617022) - 773645004 -> 86073008 (116680003) View
116680003 \|Is a (attribute)\|	86073008 \|Hypersomatotropic gigantism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624619020) - 773645004 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624620025) - 773645004 -> 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 (10624622022) - 773645004 -> 3658006 (246454002) View
246454002 \|Occurrence (attribute)\|	3658006 \|Infancy (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10624623028) - 773645004 -> 48707006 (116676008) View
116676008 \|Associated morphology (attribute)\|	48707006 \|Growth acceleration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1162984000 View
1162984000	X-linked dominant hereditary disease (disorder)	X-linked dominant hereditary disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363070008 View
363070008	Developmental hereditary disorder (disorder)	Developmental hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
86073008 View
86073008	Hypersomatotropic gigantism (disorder)	Launois syndrome	900000000000073002 \|Sufficiently defined by necessary conditions 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
789187001 View
789187001	X-linked acrogigantism due to xq26 microduplication (disorder)	Chromosome xq26 microduplication syndrome	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 (bbf1e16d-dd7c-5b87-a451-fcdb018aabce) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E22.0	TRUE	ALWAYS E22.0 \| 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)\|

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