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Terminology chevron_right Concepts chevron_right 702378002

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Component

702378002

The component that hold information about this concept.

Fully Specified Name (FSN)

Hyperparathyroidism-jaw tumor syndrome (disorder)

Shortest Term

Hyperparathyroidism 2

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

Hyperparathyroidism-jaw tumor syndrome (disorder)

SCTID: 702378002, Primitive, Active

702378002|Hyperparathyroidism-jaw tumor syndrome (disorder)|

en Familial cystic parathyroid adenomatosis
en Familial primary hyperparathyroidism with multiple ossifying jaw fibromas
en Hyperparathyroidism 2
en Hyperparathyroidism-jaw tumor syndrome
en Hyperparathyroidism-jaw tumor syndrome (disorder)
en Hyperparathyroidism-jaw tumour syndrome

Expression

702378002 |Hyperparathyroidism-jaw tumor syndrome (disorder)|
 <<< 237653008 |Familial primary hyperparathyroidism (disorder)| + 
363104002 |Hereditary disorder of endocrine system (disorder)| + 
11164009 |Autosomal dominant hereditary disorder (disorder)| + 
126634001 |Neoplasm of jaw (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 108369006 |Neoplasm (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 661005 |Jaw region structure (body structure)| }
        { 363713009 |Has interpretation (attribute)| = 35105006 |Increased (qualifier value)|,
363714003 |Interprets (attribute)| = 60877009 |Hormone secretion, function (observable entity)| }
        { 363698007 |Finding site (attribute)| = 111002 |Parathyroid structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3008592016 - Familial cystic parathyroid adenomatosis (en) View
3008592016	en	Synonym (core metadata concept)	Familial cystic parathyroid adenomatosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
2995586019 - Familial primary hyperparathyroidism with multiple ossifying jaw fibromas (en) View
2995586019	en	Synonym (core metadata concept)	Familial primary hyperparathyroidism with multiple ossifying jaw fibromas	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
2995190010 - Hyperparathyroidism 2 (en) View
2995190010	en	Synonym (core metadata concept)	Hyperparathyroidism 2	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
2995510018 - Hyperparathyroidism-jaw tumor syndrome (en) View
2995510018	en	Synonym (core metadata concept)	Hyperparathyroidism-jaw tumor syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2995355014 - Hyperparathyroidism-jaw tumor syndrome (disorder) (en) View
2995355014	en	Fully specified name (core metadata concept)	Hyperparathyroidism-jaw tumor syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
2995404015 - Hyperparathyroidism-jaw tumour syndrome (en) View
2995404015	en	Synonym (core metadata concept)	Hyperparathyroidism-jaw tumour syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (7112306026) - 702378002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7112307024) - 702378002 -> 111002 (363698007) View
363698007 \|Finding site (attribute)\|	111002 \|Parathyroid structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12894805024) - 702378002 -> 126634001 (116680003) View
116680003 \|Is a (attribute)\|	126634001 \|Neoplasm of jaw (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12894806020) - 702378002 -> 661005 (363698007) View
363698007 \|Finding site (attribute)\|	661005 \|Jaw region structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12894807027) - 702378002 -> 108369006 (116676008) View
116676008 \|Associated morphology (attribute)\|	108369006 \|Neoplasm (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12894808021) - 702378002 -> 111002 (363698007) View
363698007 \|Finding site (attribute)\|	111002 \|Parathyroid structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4968269020) - 702378002 -> 83649006 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	83649006 \|Increased hormone secretion (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9287246024) - 702378002 -> 35105006 (363713009) View
363713009 \|Has interpretation (attribute)\|	35105006 \|Increased (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9287247026) - 702378002 -> 60877009 (363714003) View
363714003 \|Interprets (attribute)\|	60877009 \|Hormone secretion, function (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4968268028) - 702378002 -> 111002 (363698007) View
363698007 \|Finding site (attribute)\|	111002 \|Parathyroid structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4968265025) - 702378002 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4968266029) - 702378002 -> 363104002 (116680003) View
116680003 \|Is a (attribute)\|	363104002 \|Hereditary disorder of endocrine system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4968267022) - 702378002 -> 237653008 (116680003) View
116680003 \|Is a (attribute)\|	237653008 \|Familial primary hyperparathyroidism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
126634001 View
126634001	Neoplasm of jaw (disorder)	Neoplasm of jaw	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
237653008 View
237653008	Familial primary hyperparathyroidism (disorder)	Familial hyperparathyroidism	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

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 (3cbc2bb7-7746-51e2-a2aa-86fa9ff10493) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E21.0	TRUE	ALWAYS E21.0	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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