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Terminology chevron_right Concepts chevron_right 1141661004

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Component

1141661004

The component that hold information about this concept.

Fully Specified Name (FSN)

Neurocutaneous melanosis (disorder)

Shortest Term

Neurocutaneous 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

Neurocutaneous melanosis (disorder)

SCTID: 1141661004, Defined, Active

1141661004|Neurocutaneous melanosis (disorder)|

en Neurocutaneous melanosis
en Neurocutaneous melanosis (disorder)

Expression

1141661004 |Neurocutaneous melanosis (disorder)|
 === 92048008 |Benign neoplasm of central nervous system (disorder)| + 
128124001 |Congenital anomaly of central nervous system (disorder)| + 
398943008 |Congenital pigmented melanocytic nevus of skin (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 1163403006 |Pigmented nevus (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 21483005 |Structure of central nervous system (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 1163403006 |Pigmented nevus (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 39937001 |Skin 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
4534966012 - Neurocutaneous melanosis (en) View
4534966012	en	Synonym (core metadata concept)	Neurocutaneous melanosis	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
4534967015 - Neurocutaneous melanosis (disorder) (en) View
4534967015	en	Fully specified name (core metadata concept)	Neurocutaneous melanosis (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (14963677023) - 1141661004 -> 1163403006 (116676008) View
116676008 \|Associated morphology (attribute)\|	1163403006 \|Pigmented nevus (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15803756029) - 1141661004 -> 400151006 (116676008) View
116676008 \|Associated morphology (attribute)\|	400151006 \|Congenital melanocytic nevus (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15803757022) - 1141661004 -> 400151006 (116676008) View
116676008 \|Associated morphology (attribute)\|	400151006 \|Congenital melanocytic nevus (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16385191028) - 1141661004 -> 1163403006 (116676008) View
116676008 \|Associated morphology (attribute)\|	1163403006 \|Pigmented nevus (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13642631023) - 1141661004 -> 299735001 (116680003) View
116680003 \|Is a (attribute)\|	299735001 \|Neurological lesion (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13642632027) - 1141661004 -> 80690008 (116680003) View
116680003 \|Is a (attribute)\|	80690008 \|Degenerative disease of the central nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13642633021) - 1141661004 -> 86042009 (116680003) View
116680003 \|Is a (attribute)\|	86042009 \|Congenital melanosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13642634026) - 1141661004 -> 15758002 (116680003) View
116680003 \|Is a (attribute)\|	15758002 \|Disorder of meninges (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13642636029) - 1141661004 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13642638028) - 1141661004 -> 1231004 (363698007) View
363698007 \|Finding site (attribute)\|	1231004 \|Meninges structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13642639020) - 1141661004 -> 48010006 (116676008) View
116676008 \|Associated morphology (attribute)\|	48010006 \|Melanosis (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15803265024) - 1141661004 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15803804029) - 1141661004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15803805028) - 1141661004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15804055026) - 1141661004 -> 128124001 (116680003) View
116680003 \|Is a (attribute)\|	128124001 \|Congenital anomaly of central nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15804056025) - 1141661004 -> 92048008 (116680003) View
116680003 \|Is a (attribute)\|	92048008 \|Benign neoplasm of central nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15804057023) - 1141661004 -> 21483005 (363698007) View
363698007 \|Finding site (attribute)\|	21483005 \|Structure of central nervous system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13642635025) - 1141661004 -> 400101001 (116676008) View
116676008 \|Associated morphology (attribute)\|	400101001 \|Melanocytic nevus - category (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13642630024) - 1141661004 -> 398943008 (116680003) View
116680003 \|Is a (attribute)\|	398943008 \|Congenital pigmented melanocytic nevus of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13642637022) - 1141661004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (13642640022) - 1141661004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
398943008 View
398943008	Congenital pigmented melanocytic nevus of skin (disorder)	Congenital pigmented nevus of skin	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
92048008 View
92048008	Benign neoplasm of central nervous system (disorder)	Benign neoplasm of central nervous system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
128124001 View
128124001	Congenital anomaly of central nervous system (disorder)	Congenital anomaly of central nervous system	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 (e1a360e2-d613-534e-ae41-f96d48322fd6) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	D22.9	TRUE	ALWAYS D22.9 \| POSSIBLE REQUIREMENT FOR MORPHOLOGY CODE	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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