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Terminology chevron_right Concepts chevron_right 82837002

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Component

82837002

The component that hold information about this concept.

Fully Specified Name (FSN)

Kenny syndrome (disorder)

Shortest Term

Kenny 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

Kenny syndrome (disorder)

SCTID: 82837002, Primitive, Active

82837002|Kenny syndrome (disorder)|

en Kenny syndrome (disorder)
en Kenny-caffey syndrome
en Kenny syndrome

Expression

82837002 |Kenny syndrome (disorder)|
 <<< 105985007 |Osteochondrodysplasia syndrome (disorder)| + 
237654002 |Idiopathic hypoparathyroidism (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 363713009 |Has interpretation (attribute)| = 1250004 |Decreased (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
824343010 - Kenny syndrome (disorder) (en) View
824343010	en	Fully specified name (core metadata concept)	Kenny syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
505290013 - Kenny-Caffey syndrome (en) View
505290013	en	Synonym (core metadata concept)	Kenny-Caffey syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
137411019 - Kenny syndrome (en) View
137411019	en	Synonym (core metadata concept)	Kenny syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (881404026) - 82837002 -> 111002 (363698007) View
363698007 \|Finding site (attribute)\|	111002 \|Parathyroid structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5020715020) - 82837002 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10527808029) - 82837002 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10527809021) - 82837002 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2044823029) - 82837002 -> 42497006 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	42497006 \|Decreased hormone secretion (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9300091020) - 82837002 -> 60877009 (363714003) View
363714003 \|Interprets (attribute)\|	60877009 \|Hormone secretion, function (observable entity)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9300092029) - 82837002 -> 1250004 (363713009) View
363713009 \|Has interpretation (attribute)\|	1250004 \|Decreased (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (881402027) - 82837002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2270485026) - 82837002 -> 112635002 (116676008) View
116676008 \|Associated morphology (attribute)\|	112635002 \|Congenital malformation (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4997545029) - 82837002 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2044821027) - 82837002 -> 40052002 (116680003) View
116680003 \|Is a (attribute)\|	40052002 \|Congenital anomaly of neck (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2044822023) - 82837002 -> 4184009 (116680003) View
116680003 \|Is a (attribute)\|	4184009 \|Congenital anomaly of endocrine gland (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (282713024) - 82837002 -> 65274008 (116680003) View
116680003 \|Is a (attribute)\|	65274008 \|Congenital anomaly of parathyroid glands (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (881403021) - 82837002 -> 127944005 (363698007) View
363698007 \|Finding site (attribute)\|	127944005 \|Entire endocrine gonad (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (881405025) - 82837002 -> 47563007 (363714003) View
363714003 \|Interprets (attribute)\|	47563007 \|Nutritional deficiency (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (282711021) - 82837002 -> 105985007 (116680003) View
116680003 \|Is a (attribute)\|	105985007 \|Osteochondrodysplasia syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (282712025) - 82837002 -> 237654002 (116680003) View
116680003 \|Is a (attribute)\|	237654002 \|Idiopathic hypoparathyroidism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
237654002 View
237654002	Idiopathic hypoparathyroidism (disorder)	Idiopathic hypoparathyroidism	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
105985007 View
105985007	Osteochondrodysplasia syndrome (disorder)	Osteochondrodysplasia syndrome	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 (20a0105c-ae4f-5efa-9529-5fadc0a4febc) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q87.8	TRUE	ALWAYS Q87.8	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)\|

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