dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 64855000

Production

add

Component

64855000

The component that hold information about this concept.

Fully Specified Name (FSN)

Pelizaeus-merzbacher disease (disorder)

Shortest Term

Sudanophilic leukodystrophy

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

Pelizaeus-merzbacher disease (disorder)

SCTID: 64855000, Primitive, Active

64855000|Pelizaeus-merzbacher disease (disorder)|

en Sudanophilic leukodystrophy
en Pelizaeus-merzbacher disease (disorder)
en Pelizaeus-merzbacher disease

Expression

64855000 |Pelizaeus-merzbacher disease (disorder)|
 <<< 192781003 |Leukodystrophy (disorder)| + 
106018006 |Hereditary degenerative disease of central nervous system (disorder)| + 
128430005 |X-linked hereditary disease (disorder)| + 
363070008 |Developmental hereditary disorder (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 125495003 |Myelin sheath alteration (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 54115001 |Myelinated nerve fiber structure (body structure)|,
370135005 |Pathological process (attribute)| = 308490002 |Pathological developmental process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 4720007 |Dystrophy (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 389080008 |White matter structure of brain and spinal cord (body structure)|,
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
107801015 - Sudanophilic leukodystrophy (en) View
107801015	en	Synonym (core metadata concept)	Sudanophilic leukodystrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
804294011 - Pelizaeus-Merzbacher disease (disorder) (en) View
804294011	en	Fully specified name (core metadata concept)	Pelizaeus-Merzbacher disease (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True
107800019 - Pelizaeus-Merzbacher disease (en) View
107800019	en	Synonym (core metadata concept)	Pelizaeus-Merzbacher disease	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (12085867027) - 64855000 -> 5294002 (116680003) View
116680003 \|Is a (attribute)\|	5294002 \|Developmental disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13068905027) - 64855000 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (253604027) - 64855000 -> 128190004 (116680003) View
116680003 \|Is a (attribute)\|	128190004 \|Inherited metabolic disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (253605026) - 64855000 -> 307360006 (116680003) View
116680003 \|Is a (attribute)\|	307360006 \|Leucodystrophy without a known biochemical basis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (835851026) - 64855000 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (835852022) - 64855000 -> 17815009 (116676008) View
116676008 \|Associated morphology (attribute)\|	17815009 \|Sudanophilic stain reaction (morphologic abnormality)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2549620023) - 64855000 -> 23585005 (116680003) View
116680003 \|Is a (attribute)\|	23585005 \|Disorder of lysosomal enzyme (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12085866020) - 64855000 -> 192781003 (116680003) View
116680003 \|Is a (attribute)\|	192781003 \|Leukodystrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12085868021) - 64855000 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12085869029) - 64855000 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12085870028) - 64855000 -> 106018006 (116680003) View
116680003 \|Is a (attribute)\|	106018006 \|Hereditary degenerative disease of central nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (12085871029) - 64855000 -> 128430005 (116680003) View
116680003 \|Is a (attribute)\|	128430005 \|X-linked hereditary disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3291818025) - 64855000 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3443002026) - 64855000 -> 25087005 (363698007) View
363698007 \|Finding site (attribute)\|	25087005 \|Structure of nervous system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9474724026) - 64855000 -> 389080008 (363698007) View
363698007 \|Finding site (attribute)\|	389080008 \|White matter structure of brain and spinal cord (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9474725025) - 64855000 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9474726029) - 64855000 -> 54115001 (363698007) View
363698007 \|Finding site (attribute)\|	54115001 \|Myelinated nerve fiber structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (835850025) - 64855000 -> 25087005 (363698007) View
363698007 \|Finding site (attribute)\|	25087005 \|Structure of nervous system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2599500028) - 64855000 -> 125495003 (116676008) View
116676008 \|Associated morphology (attribute)\|	125495003 \|Myelin sheath alteration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2599501029) - 64855000 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3291817024) - 64855000 -> 125495003 (116676008) View
116676008 \|Associated morphology (attribute)\|	125495003 \|Myelin sheath alteration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
363070008 View
363070008	Developmental hereditary disorder (disorder)	Developmental hereditary disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
106018006 View
106018006	Hereditary degenerative disease of central nervous system (disorder)	Hereditary degenerative disease of central nervous system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
128430005 View
128430005	X-linked hereditary disease (disorder)	X-linked hereditary disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
192781003 View
192781003	Leukodystrophy (disorder)	Leucodystrophy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1003447007 View
1003447007	Pelizaeus-merzbacher disease null syndrome (disorder)	Null syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1003881009 View
1003881009	Pelizaeus-merzbacher disease in female carrier (disorder)	Pelizaeus-merzbacher disease in female carrier	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
59636002 View
59636002	Pelizaeus-merzbacher disease, connatal variant (disorder)	Pelizaeus-merzbacher disease, connatal variant	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
87607002 View
87607002	Pelizaeus-merzbacher disease, classic form (disorder)	Pelizaeus-merzbacher disease, classic form	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
230368002 View
230368002	Type iii transitional pelizaeus-merzbacher disease (disorder)	Type iii transitional pelizaeus-merzbacher disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
230369005 View
230369005	Type iv adult pelizaeus-merzbacher disease (disorder)	Type iv adult pelizaeus-merzbacher disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
230370006 View
230370006	Type v atypical pelizaeus-merzbacher disease (disorder)	Type v atypical pelizaeus-merzbacher disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
230371005 View
230371005	Type vi cockayne pelizaeus-merzbacher disease (disorder)	Type vi cockayne pelizaeus-merzbacher disease	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 (81a2fe25-1d10-5162-881d-b663eaf559d4) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	E75.2	TRUE	ALWAYS E75.2	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)\|

Terminology chevron_right Concepts chevron_right 64855000

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches