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Terminology chevron_right Concepts chevron_right 75065003

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Component

75065003

The component that hold information about this concept.

Fully Specified Name (FSN)

Endemic cretinism (disorder)

Shortest Term

Cretinism

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

Endemic cretinism (disorder)

SCTID: 75065003, Defined, Active

75065003|Endemic cretinism (disorder)|

en Endemic cretinism
en Endemic cretinism (disorder)

Expression

75065003 |Endemic cretinism (disorder)|
 === 217710005 |Congenital iodine deficiency syndrome (disorder)| + 
86820007 |Endemic disease (finding)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (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
502894017 - Endemic cretinism - hypothyroid (en) View
502894017	en	Synonym (core metadata concept)	Endemic cretinism - hypothyroid	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	False
124678011 - Endemic cretinism (en) View
124678011	en	Synonym (core metadata concept)	Endemic cretinism	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
815633013 - Endemic cretinism (disorder) (en) View
815633013	en	Fully specified name (core metadata concept)	Endemic cretinism (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
502892018 - Cretinism (en) View
502892018	en	Synonym (core metadata concept)	Cretinism	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
502893011 - CHT - Congenital hypothyroidism (en) View
502893011	en	Synonym (core metadata concept)	CHT - Congenital hypothyroidism	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	False
502888013 - Congenital hypothyroidism (en) View
502888013	en	Synonym (core metadata concept)	Congenital hypothyroidism	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
502889017 - Congenital hypothyroidism not due to iodine deficiency (en) View
502889017	en	Synonym (core metadata concept)	Congenital hypothyroidism not due to iodine deficiency	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
502890014 - Congenital iodine deficiency hypothyroidism (en) View
502890014	en	Synonym (core metadata concept)	Congenital iodine deficiency hypothyroidism	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
502891013 - Congenital iodine deficiency syndrome (en) View
502891013	en	Synonym (core metadata concept)	Congenital iodine deficiency syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
502895016 - Congenital iodine deficiency syndrome - myxedematous type (en) View
502895016	en	Synonym (core metadata concept)	Congenital iodine deficiency syndrome - myxedematous type	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
502897012 - Congenital iodine deficiency syndrome - myxoedematous type (en) View
502897012	en	Synonym (core metadata concept)	Congenital iodine deficiency syndrome - myxoedematous type	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
502896015 - Endemic cretinism - myxedematous type (en) View
502896015	en	Synonym (core metadata concept)	Endemic cretinism - myxedematous type	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
502898019 - Endemic cretinism - myxoedematous type (en) View
502898019	en	Synonym (core metadata concept)	Endemic cretinism - myxoedematous type	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (5029492025) - 75065003 -> 190268003 (116680003) View
116680003 \|Is a (attribute)\|	190268003 \|Congenital hypothyroidism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13904135028) - 75065003 -> 86820007 (116680003) View
116680003 \|Is a (attribute)\|	86820007 \|Endemic disease (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (861254026) - 75065003 -> 69748006 (363698007) View
363698007 \|Finding site (attribute)\|	69748006 \|Thyroid structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12090699020) - 75065003 -> 69748006 (363698007) View
363698007 \|Finding site (attribute)\|	69748006 \|Thyroid structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5019851027) - 75065003 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10534180022) - 75065003 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10534181021) - 75065003 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (861251023) - 75065003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1681941026) - 75065003 -> 40930008 (116680003) View
116680003 \|Is a (attribute)\|	40930008 \|Hypothyroidism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2269821021) - 75065003 -> 112635002 (116676008) View
116676008 \|Associated morphology (attribute)\|	112635002 \|Congenital malformation (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4995613025) - 75065003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (861252027) - 75065003 -> 43451003 (116676008) View
116676008 \|Associated morphology (attribute)\|	43451003 \|Congenital deficiency (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2601160020) - 75065003 -> 238121000 (42752001) View
42752001 \|Due to (attribute)\|	238121000 \|Iodine deficiency (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1777591023) - 75065003 -> 238121000 (363715002) View
363715002 \|Associated etiologic finding (attribute)\|	238121000 \|Iodine deficiency (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (270051029) - 75065003 -> 40052002 (116680003) View
116680003 \|Is a (attribute)\|	40052002 \|Congenital anomaly of neck (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (270053026) - 75065003 -> 57544002 (116680003) View
116680003 \|Is a (attribute)\|	57544002 \|Multiple malformation syndrome due to non-infectious environmental agents (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (270054021) - 75065003 -> 4184009 (116680003) View
116680003 \|Is a (attribute)\|	4184009 \|Congenital anomaly of endocrine gland (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (270055022) - 75065003 -> 237562002 (116680003) View
116680003 \|Is a (attribute)\|	237562002 \|Iodine deficiency syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (861253021) - 75065003 -> 44588005 (246075003) View
246075003 \|Causative agent (attribute)\|	44588005 \|Iodine (substance)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (861255025) - 75065003 -> 127944005 (363698007) View
363698007 \|Finding site (attribute)\|	127944005 \|Entire endocrine gonad (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (861256029) - 75065003 -> 37877001 (246075003) View
246075003 \|Causative agent (attribute)\|	37877001 \|Environmental agent (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (270052020) - 75065003 -> 217710005 (116680003) View
116680003 \|Is a (attribute)\|	217710005 \|Congenital iodine deficiency syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
217710005 View
217710005	Congenital iodine deficiency syndrome (disorder)	Cretinism	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
86820007 View
86820007	Endemic disease (finding)	Endemic disease	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
237566004 View
237566004	Congenital iodine deficiency syndrome - neurological type (disorder)	Endemic cretinism - neurological type	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 (630802fd-1f47-5450-b06f-9480f680e236) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E00.9	TRUE	ALWAYS E00.9 \| 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)\|
ExtendedMap object (70627f70-b1a1-58e8-be17-b64efbed96f6) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E00.0	IFA 237566004 \| Congenital iodine deficiency syndrome - neurological type (disorder) \|	IF CONGENITAL IODINE DEFICIENCY SYNDROME - NEUROLOGICAL TYPE CHOOSE E00.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (84dbfeaf-4db7-5544-bbc3-dde3626278d1) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E00.9	OTHERWISE TRUE	ALWAYS E00.9	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 (902b52f0-507d-56e6-9214-3dc397e93813) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E00.1	IFA 440092001 \| Endemic congenital iodine deficiency syndrome of myxedematous type (disorder) \|	IF ENDEMIC CONGENITAL IODINE DEFICIENCY SYNDROME OF MYXEDEMATOUS TYPE CHOOSE E00.1 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (c58f1c43-b675-58ed-9f1d-4b0faf7383c7) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E00.2	IFA 237565000 \| Congenital iodine deficiency syndrome - mixed type (disorder) \|	IF CONGENITAL IODINE DEFICIENCY SYNDROME - MIXED TYPE CHOOSE E00.2 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (630802fd-1f47-5450-b06f-9480f680e236) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E00.9	TRUE	ALWAYS E00.9 \| 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)\|
ExtendedMap object (70627f70-b1a1-58e8-be17-b64efbed96f6) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E00.0	IFA 237566004 \| Congenital iodine deficiency syndrome - neurological type (disorder) \|	IF CONGENITAL IODINE DEFICIENCY SYNDROME - NEUROLOGICAL TYPE CHOOSE E00.0 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (84dbfeaf-4db7-5544-bbc3-dde3626278d1) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E00.9	OTHERWISE TRUE	ALWAYS E00.9	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 (902b52f0-507d-56e6-9214-3dc397e93813) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E00.1	IFA 440092001 \| Endemic congenital iodine deficiency syndrome of myxedematous type (disorder) \|	IF ENDEMIC CONGENITAL IODINE DEFICIENCY SYNDROME OF MYXEDEMATOUS TYPE CHOOSE E00.1 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|
ExtendedMap object (c58f1c43-b675-58ed-9f1d-4b0faf7383c7) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E00.2	IFA 237565000 \| Congenital iodine deficiency syndrome - mixed type (disorder) \|	IF CONGENITAL IODINE DEFICIENCY SYNDROME - MIXED TYPE CHOOSE E00.2 \| MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447639009 \|Map of source concept is context dependent (foundation metadata concept)\|

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