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Terminology chevron_right Concepts chevron_right 4184009

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Component

4184009

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital anomaly of endocrine gland (disorder)

Shortest Term

Congenital anomaly of endocrine gland

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 anomaly of endocrine gland (disorder)

SCTID: 4184009, Defined, Active

4184009|Congenital anomaly of endocrine gland (disorder)|

en Congenital anomaly of endocrine gland
en Congenital anomaly of endocrine gland (disorder)
en Congenital anomaly of endocrine organ
en Congenital malformation of the endocrine glands

Expression

4184009 |Congenital anomaly of endocrine gland (disorder)|
 === 362969004 |Disorder of endocrine system (disorder)| + 
276654001 |Congenital malformation (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 387910009 |Endocrine gland 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
8466010 - Congenital anomaly of endocrine gland (en) View
8466010	en	Synonym (core metadata concept)	Congenital anomaly of endocrine gland	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
778674010 - Congenital anomaly of endocrine gland (disorder) (en) View
778674010	en	Fully specified name (core metadata concept)	Congenital anomaly of endocrine gland (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
8469015 - Congenital anomaly of endocrine organ (en) View
8469015	en	Synonym (core metadata concept)	Congenital anomaly of endocrine organ	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
1229800012 - Congenital malformation of the endocrine glands (en) View
1229800012	en	Synonym (core metadata concept)	Congenital malformation of the endocrine glands	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
8467018 - Congenital anomaly of endocrine gland, NOS (en) View
8467018	en	Synonym (core metadata concept)	Congenital anomaly of endocrine gland, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
8468011 - Congenital anomaly of endocrine organ, NOS (en) View
8468011	en	Synonym (core metadata concept)	Congenital anomaly of endocrine organ, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (4973529021) - 4184009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4973530027) - 4184009 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4973531028) - 4184009 -> 387910009 (363698007) View
363698007 \|Finding site (attribute)\|	387910009 \|Endocrine gland structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5837892028) - 4184009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (5837893022) - 4184009 -> 387910009 (363698007) View
363698007 \|Finding site (attribute)\|	387910009 \|Endocrine gland structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10531793024) - 4184009 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10531794029) - 4184009 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (776580028) - 4184009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3316218029) - 4184009 -> 387910009 (363698007) View
363698007 \|Finding site (attribute)\|	387910009 \|Endocrine gland structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3460347025) - 4184009 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3619163029) - 4184009 -> 443341004 (116680003) View
116680003 \|Is a (attribute)\|	443341004 \|Congenital anomaly (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5020372029) - 4184009 -> 276654001 (116680003) View
116680003 \|Is a (attribute)\|	276654001 \|Congenital malformation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2595805020) - 4184009 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2595806021) - 4184009 -> 387910009 (363698007) View
363698007 \|Finding site (attribute)\|	387910009 \|Endocrine gland structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1674943024) - 4184009 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1766692027) - 4184009 -> 113331007 (363698007) View
363698007 \|Finding site (attribute)\|	113331007 \|Structure of endocrine system (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (216269023) - 4184009 -> 127345001 (116680003) View
116680003 \|Is a (attribute)\|	127345001 \|Disorder of endocrine gonad (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (216270024) - 4184009 -> 78626001 (116680003) View
116680003 \|Is a (attribute)\|	78626001 \|Congenital anomaly of trunk (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (776579026) - 4184009 -> 127944005 (363698007) View
363698007 \|Finding site (attribute)\|	127944005 \|Entire endocrine gonad (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1674944029) - 4184009 -> 362969004 (116680003) View
116680003 \|Is a (attribute)\|	362969004 \|Disorder of endocrine system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
276654001 View
276654001	Congenital malformation (disorder)	Dị tật bẩm sinh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
362969004 View
362969004	Disorder of endocrine system (disorder)	Endocrinopathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
42681006 View
42681006	Islet cell hyperplasia (disorder)	Nesidioblastosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
38824008 View
38824008	Congenital anomaly of the thymus (disorder)	Congenital anomaly of the thymus	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
371118004 View
371118004	Congenital anomaly of endocrine gonad (disorder)	Congenital anomaly of endocrine gonad	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
60637003 View
60637003	Congenital anomaly of adrenal gland (disorder)	Congenital anomaly of adrenal gland	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
65274008 View
65274008	Congenital anomaly of parathyroid glands (disorder)	Congenital anomaly of parathyroid glands	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
74012004 View
74012004	Congenital anomaly of pituitary gland (disorder)	Congenital anomaly of pituitary gland	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
237617006 View
237617006	Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness (disorder)	Rogers syndrome	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 (a11e4693-c26b-574e-8952-3b2a5ad6db28) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q89.2	TRUE	ALWAYS Q89.2	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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