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Terminology chevron_right Concepts chevron_right 722064003

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Component

722064003

The component that hold information about this concept.

Fully Specified Name (FSN)

Odontoleukodystrophy (disorder)

Shortest Term

Odontoleukodystrophy

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

Odontoleukodystrophy (disorder)

SCTID: 722064003, Primitive, Active

722064003|Odontoleukodystrophy (disorder)|

en Dentoleukoencephalopathy
en Leucodystrophy with oligodontia
en Leukodystrophy with oligodontia
en Odontoleukodystrophy
en Odontoleukodystrophy (disorder)

Expression

722064003 |Odontoleukodystrophy (disorder)|
 <<< 410066003 |Congenital anomaly in number of teeth (disorder)| + 
1208933000 |4h leukodystrophy (disorder)| + 
128285007 |Chronic disease of teeth and/or supporting structures (disorder)| + 
128290005 |Chronic disease of genitourinary system (disorder)| + 
763597000 |Hereditary ataxia (disorder)| + 
78689005 |Chronic brain syndrome (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 125495003 |Myelin sheath alteration (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 54115001 |Myelinated nerve fiber structure (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 1303291008 |Abnormal number (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 302214001 |Entire tooth (body structure)|,
246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)|,
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)| }
        { 263502005 |Clinical course (attribute)| = 255314001 |Progressive (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 52618001 |Structure of pars distalis of pituitary (body structure)| }
        { 363698007 |Finding site (attribute)| = 304041004 |Gonadal endocrine structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3330441013 - Dentoleukoencephalopathy (en) View
3330441013	en	Synonym (core metadata concept)	Dentoleukoencephalopathy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3330443011 - Leucodystrophy with oligodontia (en) View
3330443011	en	Synonym (core metadata concept)	Leucodystrophy with oligodontia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3330442018 - Leukodystrophy with oligodontia (en) View
3330442018	en	Synonym (core metadata concept)	Leukodystrophy with oligodontia	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
3330440014 - Odontoleukodystrophy (en) View
3330440014	en	Synonym (core metadata concept)	Odontoleukodystrophy	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
3330439012 - Odontoleukodystrophy (disorder) (en) View
3330439012	en	Fully specified name (core metadata concept)	Odontoleukodystrophy (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (6781202025) - 722064003 -> 61295008 (116676008) View
116676008 \|Associated morphology (attribute)\|	61295008 \|Congenital abnormal number (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15888330021) - 722064003 -> 1303291008 (116676008) View
116676008 \|Associated morphology (attribute)\|	1303291008 \|Abnormal number (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6778860026) - 722064003 -> 85995004 (116680003) View
116680003 \|Is a (attribute)\|	85995004 \|Autosomal recessive hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6778861027) - 722064003 -> 192781003 (116680003) View
116680003 \|Is a (attribute)\|	192781003 \|Leukodystrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (12091492025) - 722064003 -> 106018006 (116680003) View
116680003 \|Is a (attribute)\|	106018006 \|Hereditary degenerative disease of central nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13069359025) - 722064003 -> 363070008 (116680003) View
116680003 \|Is a (attribute)\|	363070008 \|Developmental hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (13717803027) - 722064003 -> 1148766007 (116680003) View
116680003 \|Is a (attribute)\|	1148766007 \|Hereditary disorder of tooth (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15101599022) - 722064003 -> 1208933000 (116680003) View
116680003 \|Is a (attribute)\|	1208933000 \|4h leukodystrophy (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15101600020) - 722064003 -> 128285007 (116680003) View
116680003 \|Is a (attribute)\|	128285007 \|Chronic disease of teeth and/or supporting structures (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15101601024) - 722064003 -> 128290005 (116680003) View
116680003 \|Is a (attribute)\|	128290005 \|Chronic disease of genitourinary system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15101602028) - 722064003 -> 763597000 (116680003) View
116680003 \|Is a (attribute)\|	763597000 \|Hereditary ataxia (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15101603022) - 722064003 -> 78689005 (116680003) View
116680003 \|Is a (attribute)\|	78689005 \|Chronic brain syndrome (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15101604027) - 722064003 -> 255314001 (263502005) View
263502005 \|Clinical course (attribute)\|	255314001 \|Progressive (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15101605026) - 722064003 -> 52618001 (363698007) View
363698007 \|Finding site (attribute)\|	52618001 \|Structure of pars distalis of pituitary (body structure)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (15101606025) - 722064003 -> 304041004 (363698007) View
363698007 \|Finding site (attribute)\|	304041004 \|Gonadal endocrine structure (body structure)\|	6	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6778862023) - 722064003 -> 363080007 (116680003) View
116680003 \|Is a (attribute)\|	363080007 \|Digestive system hereditary disorder (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9464157024) - 722064003 -> 363235000 (116680003) View
116680003 \|Is a (attribute)\|	363235000 \|Hereditary disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (10526749025) - 722064003 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6781206027) - 722064003 -> 125495003 (116676008) View
116676008 \|Associated morphology (attribute)\|	125495003 \|Myelin sheath alteration (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6781207020) - 722064003 -> 25087005 (363698007) View
363698007 \|Finding site (attribute)\|	25087005 \|Structure of nervous system (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9464158025) - 722064003 -> 54115001 (363698007) View
363698007 \|Finding site (attribute)\|	54115001 \|Myelinated nerve fiber structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9464159022) - 722064003 -> 389080008 (363698007) View
363698007 \|Finding site (attribute)\|	389080008 \|White matter structure of brain and spinal cord (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (9464160028) - 722064003 -> 125495003 (116676008) View
116676008 \|Associated morphology (attribute)\|	125495003 \|Myelin sheath alteration (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6778863029) - 722064003 -> 410066003 (116680003) View
116680003 \|Is a (attribute)\|	410066003 \|Congenital anomaly in number of teeth (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6781203024) - 722064003 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6781204029) - 722064003 -> 302214001 (363698007) View
363698007 \|Finding site (attribute)\|	302214001 \|Entire tooth (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (6781205028) - 722064003 -> 4720007 (116676008) View
116676008 \|Associated morphology (attribute)\|	4720007 \|Dystrophy (morphologic abnormality)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1208933000 View
1208933000	4h leukodystrophy (disorder)	4h leucodystrophy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
128285007 View
128285007	Chronic disease of teeth and/or supporting structures (disorder)	Chronic disease of teeth and/or supporting structures	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
763597000 View
763597000	Hereditary ataxia (disorder)	Hereditary ataxia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
410066003 View
410066003	Congenital anomaly in number of teeth (disorder)	Congenitally anomalous tooth number	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
128290005 View
128290005	Chronic disease of genitourinary system (disorder)	Chronic disease of genitourinary system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
78689005 View
78689005	Chronic brain syndrome (disorder)	Chronic brain syndrome	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 (1aed05a1-9251-5d3b-a136-e9a44e3c9330) 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)\|
ExtendedMap object (44ea4466-81ba-575a-999b-21620f6aee3a) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	K00.0	TRUE	ALWAYS K00.0	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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