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Terminology chevron_right Concepts chevron_right 18822004

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Component

18822004

The component that hold information about this concept.

Fully Specified Name (FSN)

Centrofacial lentiginosis syndrome (disorder)

Shortest Term

Centrofacial lentiginosis

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

Centrofacial lentiginosis syndrome (disorder)

SCTID: 18822004, Primitive, Active

18822004|Centrofacial lentiginosis syndrome (disorder)|

en Centrofacial lentiginosis
en Centrofacial lentiginosis syndrome
en Centrofacial lentiginosis syndrome (disorder)

Expression

18822004 |Centrofacial lentiginosis syndrome (disorder)|
 <<< 403804008 |Hereditary hypermelanosis (disorder)| + 
86042009 |Congenital melanosis (disorder)| + 
10679391000119104 |Mass of skin of head (finding)| + 
402624000 |Lentiginosis (disorder)| + 
400083002 |Congenital hamartoma of skin (disorder)| + 
11164009 |Autosomal dominant hereditary disorder (disorder)| + 
121000119106 |Lesion of skin of face (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 767376003 |Lentigo (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 73897004 |Skin structure of face (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
1222190018 - Centrofacial lentiginosis (en) View
1222190018	en	Synonym (core metadata concept)	Centrofacial lentiginosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
31738018 - Centrofacial lentiginosis syndrome (en) View
31738018	en	Synonym (core metadata concept)	Centrofacial lentiginosis syndrome	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
746397018 - Centrofacial lentiginosis syndrome (disorder) (en) View
746397018	en	Fully specified name (core metadata concept)	Centrofacial lentiginosis syndrome (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (9358712027) - 18822004 -> 398302004 (116680003) View
116680003 \|Is a (attribute)\|	398302004 \|Congenital anomaly of face (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9358715025) - 18822004 -> 205564003 (116680003) View
116680003 \|Is a (attribute)\|	205564003 \|Congenital pigmentary skin anomalies (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10519233026) - 18822004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13068969024) - 18822004 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9358714026) - 18822004 -> 724839001 (116680003) View
116680003 \|Is a (attribute)\|	724839001 \|Genetic disorder of skin pigmentation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12209802028) - 18822004 -> 403804008 (116680003) View
116680003 \|Is a (attribute)\|	403804008 \|Hereditary hypermelanosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9358713021) - 18822004 -> 432525007 (116680003) View
116680003 \|Is a (attribute)\|	432525007 \|Mass of head (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10736989024) - 18822004 -> 10679391000119104 (116680003) View
116680003 \|Is a (attribute)\|	10679391000119104 \|Mass of skin of head (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3311370025) - 18822004 -> 41162001 (116676008) View
116676008 \|Associated morphology (attribute)\|	41162001 \|Increased melanin pigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3311371026) - 18822004 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5010355021) - 18822004 -> 399960008 (116680003) View
116680003 \|Is a (attribute)\|	399960008 \|Congenital hamartoma (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5010356022) - 18822004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5010357029) - 18822004 -> 51398009 (116676008) View
116676008 \|Associated morphology (attribute)\|	51398009 \|Hamartoma (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9358709025) - 18822004 -> 73897004 (363698007) View
363698007 \|Finding site (attribute)\|	73897004 \|Skin structure of face (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9358710024) - 18822004 -> 400083002 (116680003) View
116680003 \|Is a (attribute)\|	400083002 \|Congenital hamartoma of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9358711023) - 18822004 -> 767376003 (116676008) View
116676008 \|Associated morphology (attribute)\|	767376003 \|Lentigo (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9358716029) - 18822004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9358717022) - 18822004 -> 11164009 (116680003) View
116680003 \|Is a (attribute)\|	11164009 \|Autosomal dominant hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9358718028) - 18822004 -> 121000119106 (116680003) View
116680003 \|Is a (attribute)\|	121000119106 \|Lesion of skin of face (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9502175021) - 18822004 -> 86042009 (116680003) View
116680003 \|Is a (attribute)\|	86042009 \|Congenital melanosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (177108029) - 18822004 -> 75523000 (116680003) View
116680003 \|Is a (attribute)\|	75523000 \|Congenital hamartosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (717529020) - 18822004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2264824026) - 18822004 -> 51398009 (116676008) View
116676008 \|Associated morphology (attribute)\|	51398009 \|Hamartoma (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2786225021) - 18822004 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2786226022) - 18822004 -> 41162001 (116676008) View
116676008 \|Associated morphology (attribute)\|	41162001 \|Increased melanin pigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (717530026) - 18822004 -> 20795001 (363698007) View
363698007 \|Finding site (attribute)\|	20795001 \|Structure of skin region (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1064050029) - 18822004 -> 4830009 (116676008) View
116676008 \|Associated morphology (attribute)\|	4830009 \|Hyperpigmentation (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2225631023) - 18822004 -> 398744007 (116680003) View
116680003 \|Is a (attribute)\|	398744007 \|Lentigo (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2225632027) - 18822004 -> 238907001 (116680003) View
116680003 \|Is a (attribute)\|	238907001 \|Site-specific disorder of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2769803026) - 18822004 -> 402624000 (116680003) View
116680003 \|Is a (attribute)\|	402624000 \|Lentiginosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (177107023) - 18822004 -> 38164009 (116680003) View
116680003 \|Is a (attribute)\|	38164009 \|Congenital anomaly of integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (177109021) - 18822004 -> 75534002 (116680003) View
116680003 \|Is a (attribute)\|	75534002 \|Lentigo (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (717528028) - 18822004 -> 21119008 (116676008) View
116676008 \|Associated morphology (attribute)\|	21119008 \|Pigmented nevus, no icd-o subtype (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1064051025) - 18822004 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1690016027) - 18822004 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (717524026) - 18822004 -> 367634005 (308489006) View
308489006 \|Pathological process (qualifier value)\|	367634005 \|Benign neoplastic process (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (717526029) - 18822004 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
403804008 View
403804008	Hereditary hypermelanosis (disorder)	Hereditary hypermelanosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
10679391000119104 View
10679391000119104	Mass of skin of head (finding)	Mass of skin of head	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
86042009 View
86042009	Congenital melanosis (disorder)	Congenital melanosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
402624000 View
402624000	Lentiginosis (disorder)	Tàn nhang	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
121000119106 View
121000119106	Lesion of skin of face (disorder)	Lesion of skin of face	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
400083002 View
400083002	Congenital hamartoma of skin (disorder)	Congenital hamartoma of skin	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
11164009 View
11164009	Autosomal dominant hereditary disorder (disorder)	Ad - autosomal dominant	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 (b21a4793-c13d-5cda-a6ac-63a0dd7fd1da) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	L81.4	TRUE	ALWAYS L81.4	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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