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Terminology chevron_right Concepts chevron_right 86042009

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Component

86042009

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital melanosis (disorder)

Shortest Term

Congenital melanosis

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 melanosis (disorder)

SCTID: 86042009, Defined, Active

86042009|Congenital melanosis (disorder)|

en Congenital melanosis
en Congenital melanosis (disorder)

Expression

86042009 |Congenital melanosis (disorder)|
 === 414662006 |Melanosis (disorder)| + 
66091009 |Congenital disease (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 48010006 |Melanosis (morphologic abnormality)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
142649017 - Congenital melanosis (en) View
142649017	en	Synonym (core metadata concept)	Congenital melanosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
828223014 - Congenital melanosis (disorder) (en) View
828223014	en	Fully specified name (core metadata concept)	Congenital melanosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (889443025) - 86042009 -> 56588001 (116676008) View
116676008 \|Associated morphology (attribute)\|	56588001 \|Congenital hyperpigmentation (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5994129023) - 86042009 -> 276654001 (116680003) View
116680003 \|Is a (attribute)\|	276654001 \|Congenital malformation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5994130029) - 86042009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9502025021) - 86042009 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (889444020) - 86042009 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (889446022) - 86042009 -> 48010006 (116676008) View
116676008 \|Associated morphology (attribute)\|	48010006 \|Melanosis (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (1684207027) - 86042009 -> 199879009 (116680003) View
116680003 \|Is a (attribute)\|	199879009 \|Congenital anomaly of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2453475029) - 86042009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2525776024) - 86042009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2697956026) - 86042009 -> 414662006 (116680003) View
116680003 \|Is a (attribute)\|	414662006 \|Melanosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (889445021) - 86042009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1684208021) - 86042009 -> 95324001 (116680003) View
116680003 \|Is a (attribute)\|	95324001 \|Skin lesion (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2217587021) - 86042009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2202712020) - 86042009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1831060023) - 86042009 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (288395022) - 86042009 -> 38164009 (116680003) View
116680003 \|Is a (attribute)\|	38164009 \|Congenital anomaly of integument (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
414662006 View
414662006	Melanosis (disorder)	Melanosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
66091009 View
66091009	Congenital disease (disorder)	Congenital disease	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
897554004 View
897554004	Dermal melanocytic hamartoma (disorder)	Dermal melanocytic hamartoma	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
205583005 View
205583005	Hereditary benign acanthosis nigricans (disorder)	Hereditary benign acanthosis nigricans	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
237606005 View
237606005	Hereditary benign acanthosis nigricans with insulin resistance (disorder)	Insulin-resistant acanthosis nigricans type a	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
764995008 View
764995008	Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome (disorder)	Ectodermal dysplasia short stature syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
765195000 View
765195000	Familial generalized lentiginosis (disorder)	Familial lentigines profusa	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
720512007 View
720512007	Arterial dissection and lentiginosis syndrome (disorder)	Arterial dissection and lentiginosis syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
45795007 View
45795007	Melanosis oculi (disorder)	Melanosis oculi	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
18822004 View
18822004	Centrofacial lentiginosis syndrome (disorder)	Centrofacial lentiginosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
51174006 View
51174006	Congenital melanosis of sclera (disorder)	Congenital melanosis of sclera	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
54411001 View
54411001	Peutz-jeghers syndrome (disorder)	Perioral lentiginosis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
239089006 View
239089006	Acromelanosis (disorder)	Acromelanosis	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 (6d801696-9e3c-5251-8997-c49b630699e0) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	-	TRUE	MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447638001 \|Map source concept cannot be classified with available data (foundation metadata concept)\|

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