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Terminology chevron_right Concepts chevron_right 237516005

Production

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Component

237516005

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital thyroid hypoplasia (disorder)

Shortest Term

Congenital thyroid hypoplasia

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

Congenital thyroid hypoplasia (disorder)

SCTID: 237516005, Defined, Active

237516005|Congenital thyroid hypoplasia (disorder)|

en Congenital thyroid hypoplasia
en Congenital thyroid hypoplasia (disorder)

Expression

237516005 |Congenital thyroid hypoplasia (disorder)|
 === 32454003 |Congenital anomaly of the thyroid gland (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 55199003 |Hypoplasia (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
355959015 - Congenital thyroid hypoplasia (en) View
355959015	en	Synonym (core metadata concept)	Congenital thyroid hypoplasia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
626257014 - Congenital thyroid hypoplasia (disorder) (en) View
626257014	en	Fully specified name (core metadata concept)	Congenital thyroid hypoplasia (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (526041029) - 237516005 -> 69748006 (363698007) View
363698007 \|Finding site (attribute)\|	69748006 \|Thyroid structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (4972656020) - 237516005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4989672024) - 237516005 -> 69748006 (363698007) View
363698007 \|Finding site (attribute)\|	69748006 \|Thyroid structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5004196026) - 237516005 -> 55199003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55199003 \|Hypoplasia (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6120102025) - 237516005 -> 55199003 (116676008) View
116676008 \|Associated morphology (attribute)\|	55199003 \|Hypoplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6120103024) - 237516005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10519357028) - 237516005 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (526043026) - 237516005 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2533501022) - 237516005 -> 276654001 (116680003) View
116680003 \|Is a (attribute)\|	276654001 \|Congenital malformation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3408317020) - 237516005 -> 69748006 (363698007) View
363698007 \|Finding site (attribute)\|	69748006 \|Thyroid structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3408318026) - 237516005 -> 38146002 (116676008) View
116676008 \|Associated morphology (attribute)\|	38146002 \|Congenital hypoplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2575164026) - 237516005 -> 38146002 (116676008) View
116676008 \|Associated morphology (attribute)\|	38146002 \|Congenital hypoplasia (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (53039028) - 237516005 -> 237515009 (116680003) View
116680003 \|Is a (attribute)\|	237515009 \|Congenital hypothyroidism without goiter (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1729628023) - 237516005 -> 43451003 (116676008) View
116676008 \|Associated morphology (attribute)\|	43451003 \|Congenital deficiency (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1729629026) - 237516005 -> 238121000 (363715002) View
363715002 \|Associated etiologic finding (attribute)\|	238121000 \|Iodine deficiency (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2254055020) - 237516005 -> 112635002 (116676008) View
116676008 \|Associated morphology (attribute)\|	112635002 \|Congenital malformation (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (526042020) - 237516005 -> 127944005 (363698007) View
363698007 \|Finding site (attribute)\|	127944005 \|Entire endocrine gonad (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (53038020) - 237516005 -> 32454003 (116680003) View
116680003 \|Is a (attribute)\|	32454003 \|Congenital anomaly of the thyroid gland (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
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

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 (4ccbeaaf-af26-5ecc-bdd0-beb767933fa7) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E03.1	TRUE	ALWAYS E03.1	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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