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Terminology chevron_right Concepts chevron_right 55838005

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Component

55838005

The component that hold information about this concept.

Fully Specified Name (FSN)

Athyrotic hypothyroidism sequence (disorder)

Shortest Term

Hypothyroidism sequence

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

Athyrotic hypothyroidism sequence (disorder)

SCTID: 55838005, Primitive, Active

55838005|Athyrotic hypothyroidism sequence (disorder)|

en Athyrotic hypothyroidism sequence
en Athyrotic hypothyroidism sequence (disorder)
en Hypothyroidism sequence

Expression

55838005 |Athyrotic hypothyroidism sequence (disorder)|
 <<< 32454003 |Congenital anomaly of the thyroid gland (disorder)| + 
190268003 |Congenital hypothyroidism (disorder)| + 
105989001 |Malformation sequence (disorder)| : 
        { 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
92857017 - Athyrotic hypothyroidism sequence (en) View
92857017	en	Synonym (core metadata concept)	Athyrotic hypothyroidism sequence	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
794269013 - Athyrotic hypothyroidism sequence (disorder) (en) View
794269013	en	Fully specified name (core metadata concept)	Athyrotic hypothyroidism sequence (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
92858010 - Hypothyroidism sequence (en) View
92858010	en	Synonym (core metadata concept)	Hypothyroidism sequence	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (2693949020) - 55838005 -> 298397000 (116680003) View
116680003 \|Is a (attribute)\|	298397000 \|Lesion of neck (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3306223022) - 55838005 -> 61350003 (116676008) View
116676008 \|Associated morphology (attribute)\|	61350003 \|Surgical acquired absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4997467026) - 55838005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5020682022) - 55838005 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9619466021) - 55838005 -> 32454003 (116680003) View
116680003 \|Is a (attribute)\|	32454003 \|Congenital anomaly of the thyroid gland (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9619468022) - 55838005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10525660023) - 55838005 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10525661022) - 55838005 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (238904020) - 55838005 -> 40930008 (116680003) View
116680003 \|Is a (attribute)\|	40930008 \|Hypothyroidism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (812524024) - 55838005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2268135029) - 55838005 -> 112635002 (116676008) View
116676008 \|Associated morphology (attribute)\|	112635002 \|Congenital malformation (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5029861022) - 55838005 -> 190268003 (116680003) View
116680003 \|Is a (attribute)\|	190268003 \|Congenital hypothyroidism (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (812522023) - 55838005 -> 69748006 (363698007) View
363698007 \|Finding site (attribute)\|	69748006 \|Thyroid structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (812525020) - 55838005 -> 61350003 (116676008) View
116676008 \|Associated morphology (attribute)\|	61350003 \|Surgical acquired absence (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3306222028) - 55838005 -> 69748006 (363698007) View
363698007 \|Finding site (attribute)\|	69748006 \|Thyroid structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (238901028) - 55838005 -> 4184009 (116680003) View
116680003 \|Is a (attribute)\|	4184009 \|Congenital anomaly of endocrine gland (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (238903025) - 55838005 -> 40052002 (116680003) View
116680003 \|Is a (attribute)\|	40052002 \|Congenital anomaly of neck (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (812523029) - 55838005 -> 127944005 (363698007) View
363698007 \|Finding site (attribute)\|	127944005 \|Entire endocrine gonad (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (238902024) - 55838005 -> 105989001 (116680003) View
116680003 \|Is a (attribute)\|	105989001 \|Malformation sequence (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
32454003 View
32454003	Congenital anomaly of the thyroid gland (disorder)	Congenital anomaly of the thyroid gland	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
105989001 View
105989001	Malformation sequence (disorder)	Malformation sequence	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 (612cebe8-4186-57ac-9ff6-05658f52ca73) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E03.8	TRUE	ALWAYS E03.8	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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