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Terminology chevron_right Concepts chevron_right 64491003

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Component

64491003

The component that hold information about this concept.

Fully Specified Name (FSN)

Myxedematous form of cretinism (disorder)

Shortest Term

Congenital myxedema

Definition Status

900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Myxedematous form of cretinism (disorder)

SCTID: 64491003, Defined, Active

64491003|Myxedematous form of cretinism (disorder)|

en Congenital myxedema
en Congenital myxoedema
en Myxedematous form of cretinism
en Myxedematous form of cretinism (disorder)
en Myxoedematous form of cretinism

Expression

64491003 |Myxedematous form of cretinism (disorder)|
 === 190268003 |Congenital hypothyroidism (disorder)| + 
43153006 |Myxedema (disorder)| + 
217710005 |Congenital iodine deficiency syndrome (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 59909002 |Hard edema (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 69748006 |Thyroid structure (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
107195016 - Congenital myxedema (en) View
107195016	en	Synonym (core metadata concept)	Congenital myxedema	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
499869013 - Congenital myxoedema (en) View
499869013	en	Synonym (core metadata concept)	Congenital myxoedema	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
107194017 - Myxedematous form of cretinism (en) View
107194017	en	Synonym (core metadata concept)	Myxedematous form of cretinism	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
803890016 - Myxedematous form of cretinism (disorder) (en) View
803890016	en	Fully specified name (core metadata concept)	Myxedematous form of cretinism (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
107196015 - Myxoedematous form of cretinism (en) View
107196015	en	Synonym (core metadata concept)	Myxoedematous form of cretinism	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (4997245025) - 64491003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10515196022) - 64491003 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10515197029) - 64491003 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12085843024) - 64491003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12085844029) - 64491003 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5020577023) - 64491003 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1774092026) - 64491003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2268871026) - 64491003 -> 112635002 (116676008) View
116676008 \|Associated morphology (attribute)\|	112635002 \|Congenital malformation (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5029828026) - 64491003 -> 190268003 (116680003) View
116680003 \|Is a (attribute)\|	190268003 \|Congenital hypothyroidism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (834900027) - 64491003 -> 43451003 (116676008) View
116676008 \|Associated morphology (attribute)\|	43451003 \|Congenital deficiency (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (834901028) - 64491003 -> 69748006 (363698007) View
363698007 \|Finding site (attribute)\|	69748006 \|Thyroid structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1774090023) - 64491003 -> 59909002 (116676008) View
116676008 \|Associated morphology (attribute)\|	59909002 \|Hard edema (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3336422027) - 64491003 -> 59909002 (116676008) View
116676008 \|Associated morphology (attribute)\|	59909002 \|Hard edema (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3465945026) - 64491003 -> 69748006 (363698007) View
363698007 \|Finding site (attribute)\|	69748006 \|Thyroid structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2599433020) - 64491003 -> 238121000 (42752001) View
42752001 \|Due to (attribute)\|	238121000 \|Iodine deficiency (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1774091022) - 64491003 -> 238121000 (363715002) View
363715002 \|Associated etiologic finding (attribute)\|	238121000 \|Iodine deficiency (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (834902024) - 64491003 -> 127944005 (363698007) View
363698007 \|Finding site (attribute)\|	127944005 \|Entire endocrine gonad (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (253020020) - 64491003 -> 217710005 (116680003) View
116680003 \|Is a (attribute)\|	217710005 \|Congenital iodine deficiency syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (253021024) - 64491003 -> 43153006 (116680003) View
116680003 \|Is a (attribute)\|	43153006 \|Myxedema (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
190268003 View
190268003	Congenital hypothyroidism (disorder)	Congenital hypothyroidism	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
217710005 View
217710005	Congenital iodine deficiency syndrome (disorder)	Cretinism	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
43153006 View
43153006	Myxedema (disorder)	Myxedema	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
440092001 View
440092001	Endemic congenital iodine deficiency syndrome of myxedematous type (disorder)	Endemic cretinism - myxedematous type	900000000000073002 \|Sufficiently defined by necessary conditions 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 (41bd78eb-7a20-5b8b-b539-2b868dc463b7) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E00.1	TRUE	ALWAYS E00.1 \| 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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