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Terminology chevron_right Concepts chevron_right 33559001

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Component

33559001

The component that hold information about this concept.

Fully Specified Name (FSN)

Pineal hyperplasia and diabetes mellitus syndrome (disorder)

Shortest Term

Mendenhall syndrome

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

Pineal hyperplasia and diabetes mellitus syndrome (disorder)

SCTID: 33559001, Primitive, Active

33559001|Pineal hyperplasia and diabetes mellitus syndrome (disorder)|

en Pineal hyperplasia, insulin-resistant diabetes mellitus and somatic abnormalities
en Mendenhall syndrome
en Pineal hyperplasia and diabetes mellitus syndrome
en Pineal hyperplasia and diabetes mellitus syndrome (disorder)
en Rabson-mendenhall syndrome

Expression

33559001 |Pineal hyperplasia and diabetes mellitus syndrome (disorder)|
 <<< 609569007 |Diabetes mellitus due to genetic defect in insulin action (disorder)| + 
87536007 |Central nervous system complication (disorder)| + 
897438000 |Structural abnormality of pineal gland (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 76197007 |Hyperplasia (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 45793000 |Pineal structure (body structure)| }
        { 42752001 |Due to (attribute)| = 782964007 |Genetic disease (disorder)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
1228082013 - Pineal hyperplasia, insulin-resistant diabetes mellitus and somatic abnormalities (en) View
1228082013	en	Synonym (core metadata concept)	Pineal hyperplasia, insulin-resistant diabetes mellitus and somatic abnormalities	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
1228083015 - Pineal hyperplasia, insulin-resistant diabetes mellitus and somatic abnormalities (disorder) (en) View
1228083015	en	Synonym (core metadata concept)	Pineal hyperplasia, insulin-resistant diabetes mellitus and somatic abnormalities (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
55999015 - Mendenhall syndrome (en) View
55999015	en	Synonym (core metadata concept)	Mendenhall syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
55998011 - Pineal hyperplasia and diabetes mellitus syndrome (en) View
55998011	en	Synonym (core metadata concept)	Pineal hyperplasia and diabetes mellitus syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
55997018 - Pineal hyperplasia AND diabetes mellitus syndrome (en) View
55997018	en	Synonym (core metadata concept)	Pineal hyperplasia AND diabetes mellitus syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
764977014 - Pineal hyperplasia AND diabetes mellitus syndrome (disorder) (en) View
764977014	en	Fully specified name (core metadata concept)	Pineal hyperplasia AND diabetes mellitus syndrome (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
56000018 - Rabson-Mendenhall syndrome (en) View
56000018	en	Synonym (core metadata concept)	Rabson-Mendenhall syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (4599023027) - 33559001 -> 5969009 (116680003) View
116680003 \|Is a (attribute)\|	5969009 \|Diabetes mellitus associated with genetic syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11569215029) - 33559001 -> 782964007 (47429007) View
47429007 \|Associated with (attribute)\|	782964007 \|Genetic disease (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16409701022) - 33559001 -> 782964007 (42752001) View
42752001 \|Due to (attribute)\|	782964007 \|Genetic disease (disorder)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (202557023) - 33559001 -> 128470003 (116680003) View
116680003 \|Is a (attribute)\|	128470003 \|Pineal gland disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16381334020) - 33559001 -> 897438000 (116680003) View
116680003 \|Is a (attribute)\|	897438000 \|Structural abnormality of pineal gland (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13951466024) - 33559001 -> 87536007 (116680003) View
116680003 \|Is a (attribute)\|	87536007 \|Central nervous system complication (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4599025023) - 33559001 -> 290028006 (47429007) View
47429007 \|Associated with (attribute)\|	290028006 \|Genetic syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1673224020) - 33559001 -> 281867008 (116680003) View
116680003 \|Is a (attribute)\|	281867008 \|Multisystem disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4733356029) - 33559001 -> 609569007 (116680003) View
116680003 \|Is a (attribute)\|	609569007 \|Diabetes mellitus due to genetic defect in insulin action (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (202559021) - 33559001 -> 73211009 (116680003) View
116680003 \|Is a (attribute)\|	73211009 \|Diabetes mellitus (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (755860027) - 33559001 -> 76197007 (116676008) View
116676008 \|Associated morphology (attribute)\|	76197007 \|Hyperplasia (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (755861028) - 33559001 -> 78696007 (363698007) View
363698007 \|Finding site (attribute)\|	78696007 \|Endocrine pancreatic structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (755862024) - 33559001 -> 45793000 (363698007) View
363698007 \|Finding site (attribute)\|	45793000 \|Pineal structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4599022021) - 33559001 -> 76197007 (116676008) View
116676008 \|Associated morphology (attribute)\|	76197007 \|Hyperplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4599024022) - 33559001 -> 45793000 (363698007) View
363698007 \|Finding site (attribute)\|	45793000 \|Pineal structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3413571023) - 33559001 -> 86762007 (363698007) View
363698007 \|Finding site (attribute)\|	86762007 \|Structure of digestive system (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (202558029) - 33559001 -> 312572002 (116680003) View
116680003 \|Is a (attribute)\|	312572002 \|Multisystem disorder o-p (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (755859021) - 33559001 -> 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
897438000 View
897438000	Structural abnormality of pineal gland (disorder)	Abnormal pineal gland morphology	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
87536007 View
87536007	Central nervous system complication (disorder)	Central nervous system complication	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
609569007 View
609569007	Diabetes mellitus due to genetic defect in insulin action (disorder)	Diabetes mellitus due to genetic defect in insulin action	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 (75d6f052-e5bb-5ca5-b151-c344c9d79a04) 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 (a7625a9b-a8ed-577b-91fe-8ebeae4b4a27) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E13.6	TRUE	ALWAYS E13.6	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)\|

Terminology chevron_right Concepts chevron_right 33559001

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