dock_to_right dock_to_right arrow_back

Terminology chevron_right Concepts chevron_right 88425004

Production

add

Component

88425004

The component that hold information about this concept.

Fully Specified Name (FSN)

Congenital anomaly of nervous system (disorder)

Shortest Term

Dị tật bẩm sinh của hệ thần kinh

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 anomaly of nervous system (disorder)

SCTID: 88425004, Defined, Active

88425004|Congenital anomaly of nervous system (disorder)|

vi Dị tật bẩm sinh của hệ thần kinh
en Congenital anomaly of nervous system
en Congenital anomaly of nervous system (disorder)
en Congenital deformity of nervous system
en Congenital disease of nervous system
en Congenital lesion of nervous system
en Congenital malformation of the nervous system

Expression

88425004 |Congenital anomaly of nervous system (disorder)|
 === 118940003 |Disorder of nervous system (disorder)| + 
276654001 |Congenital malformation (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 49755003 |Morphologically abnormal structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 25087005 |Structure of nervous system (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
490631000003112 - dị tật bẩm sinh của hệ thần kinh (vi) View
490631000003112	vi	Synonym (core metadata concept)	dị tật bẩm sinh của hệ thần kinh	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
146609011 - Congenital anomaly of nervous system (en) View
146609011	en	Synonym (core metadata concept)	Congenital anomaly of nervous system	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
831106014 - Congenital anomaly of nervous system (disorder) (en) View
831106014	en	Fully specified name (core metadata concept)	Congenital anomaly of nervous system (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
146616012 - Congenital deformity of nervous system (en) View
146616012	en	Synonym (core metadata concept)	Congenital deformity of nervous system	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
146614010 - Congenital disease of nervous system (en) View
146614010	en	Synonym (core metadata concept)	Congenital disease of nervous system	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
146615011 - Congenital lesion of nervous system (en) View
146615011	en	Synonym (core metadata concept)	Congenital lesion of nervous system	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
508025017 - Congenital malformation of the nervous system (en) View
508025017	en	Synonym (core metadata concept)	Congenital malformation of the nervous system	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Acceptable	True
146610018 - Congenital anomaly of nervous system, NOS (en) View
146610018	en	Synonym (core metadata concept)	Congenital anomaly of nervous system, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
146613016 - Congenital deformity of nervous system, NOS (en) View
146613016	en	Synonym (core metadata concept)	Congenital deformity of nervous system, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
146611019 - Congenital disease of nervous system, NOS (en) View
146611019	en	Synonym (core metadata concept)	Congenital disease of nervous system, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
146612014 - Congenital lesion of nervous system, NOS (en) View
146612014	en	Synonym (core metadata concept)	Congenital lesion of nervous system, NOS	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (896055028) - 88425004 -> 25087005 (363698007) View
363698007 \|Finding site (attribute)\|	25087005 \|Structure of nervous system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2552219027) - 88425004 -> 118940003 (116680003) View
116680003 \|Is a (attribute)\|	118940003 \|Disorder of nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2772468027) - 88425004 -> 230764002 (116680003) View
116680003 \|Is a (attribute)\|	230764002 \|Congenital and developmental anomalies of the nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4976984026) - 88425004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4976985025) - 88425004 -> 21390004 (116676008) View
116676008 \|Associated morphology (attribute)\|	21390004 \|Developmental anomaly (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (4976986029) - 88425004 -> 25087005 (363698007) View
363698007 \|Finding site (attribute)\|	25087005 \|Structure of nervous system (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (6091069021) - 88425004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10514132025) - 88425004 -> 49755003 (116676008) View
116676008 \|Associated morphology (attribute)\|	49755003 \|Morphologically abnormal structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (10514133024) - 88425004 -> 308490002 (370135005) View
370135005 \|Pathological process (attribute)\|	308490002 \|Pathological developmental process (qualifier value)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (896056027) - 88425004 -> 255399007 (246454002) View
246454002 \|Occurrence (attribute)\|	255399007 \|Congenital (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3291783022) - 88425004 -> 25087005 (363698007) View
363698007 \|Finding site (attribute)\|	25087005 \|Structure of nervous system (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3447002025) - 88425004 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3619607026) - 88425004 -> 443341004 (116680003) View
116680003 \|Is a (attribute)\|	443341004 \|Congenital anomaly (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (5019781026) - 88425004 -> 276654001 (116680003) View
116680003 \|Is a (attribute)\|	276654001 \|Congenital malformation (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2603460022) - 88425004 -> 107656002 (116676008) View
116676008 \|Associated morphology (attribute)\|	107656002 \|Congenital anomaly (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (292487027) - 88425004 -> 66091009 (116680003) View
116680003 \|Is a (attribute)\|	66091009 \|Congenital disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2698212020) - 88425004 -> 299735001 (116680003) View
116680003 \|Is a (attribute)\|	299735001 \|Neurological lesion (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (292486020) - 88425004 -> 230764002 (116680003) View
116680003 \|Is a (attribute)\|	230764002 \|Congenital and developmental anomalies of the nervous system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
276654001 View
276654001	Congenital malformation (disorder)	Dị tật bẩm sinh	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
118940003 View
118940003	Disorder of nervous system (disorder)	Neurological disorder	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
1144624009 View
1144624009	Congenital absence of myelination of peripheral nerve (disorder)	Peripheral amyelination	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
230794008 View
230794008	Neuronal choristoma (disorder)	Neuronal choristoma	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
266673001 View
266673001	Ectopic neuronal tissue (disorder)	Ectopic grey matter	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
782739000 View
782739000	Male emopamil-binding protein disorder with neurological defect (disorder)	Male emopamil-binding protein disorder with neurological defect	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
253098009 View
253098009	Neural tube defect (disorder)	Neural tube defect	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
771473004 View
771473004	Papular epidermal nevi with skyline basal cell layers syndrome (disorder)	Pens syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
765434008 View
765434008	Human immunodeficiency virus type i enhancer binding protein 2 related intellectual disability (disorder)	Hivep2-related intellectual disability	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
766931003 View
766931003	Hypomyelination neuropathy arthrogryposis syndrome (disorder)	Hypomyelination neuropathy arthrogryposis syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
724091002 View
724091002	Neuroectodermal melanolysosomal disease (disorder)	Elejalde disease	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
733469003 View
733469003	Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome (disorder)	Westerhof beemer cormane syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
722996009 View
722996009	Congenital malformation of autonomic nervous system (disorder)	Congenital malformation of autonomic nervous system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
230502003 View
230502003	Congenital anosmia (disorder)	Congenital anosmia	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
287080001 View
287080001	Congenital anomaly of nervous system of head/neck (disorder)	Congenital anomaly of nervous system of head/neck	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
22133005 View
22133005	Congenital anomaly of the peripheral nervous system (disorder)	Congenital anomaly of the peripheral nervous system	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
111338006 View
111338006	Agenesis of nerve (disorder)	Nerve agenesis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
403775003 View
403775003	Hereditary neurocutaneous angiomata (disorder)	Hereditary neurocutaneous angiomata	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
23150001 View
23150001	Proteus syndrome (disorder)	Proteus syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
27642008 View
27642008	Dysmorphic sialidosis, congenital form (disorder)	Dysmorphic sialidosis, congenital form	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
36025004 View
36025004	Fibrous skin tumor of tuberous sclerosis (disorder)	Pringle tumor	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
40354009 View
40354009	De lange syndrome (disorder)	Amsterdam dwarf	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
41283003 View
41283003	Cerebro-oculo-facio-skeletal syndrome (disorder)	Cofs syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
69664005 View
69664005	Ecchordosis physaliphora (disorder)	Ecchordosis physaliphora	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
75968004 View
75968004	Sotos' syndrome (disorder)	Soto syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
76880004 View
76880004	Angelman syndrome (disorder)	Angelman syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
93559003 View
93559003	Hypogonadism with anosmia (disorder)	Kallman syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
95477007 View
95477007	Congenital degeneration of nervous system (disorder)	Congenital neurological degeneration	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
95652003 View
95652003	Congenital flaccid paralysis (disorder)	Congenital flaccid paralysis	900000000000074008 \|Necessary but not sufficient concept 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
230562000 View
230562000	Congenital hypomyelinating neuropathy (disorder)	Lyon's hypomyelinating neuropathy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
233718008 View
233718008	Pulmonary tuberose sclerosis (disorder)	Xơ lao phổi	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
253128003 View
253128003	Abnormality of neurogenesis (disorder)	Abnormality of neurogenesis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
363034005 View
363034005	Congenital anomaly of neural structure of trunk (disorder)	Congenital anomaly of neural structure of trunk	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 (53d4c4a4-b22a-592e-a05a-c20b9a8ca2eb) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	Q07.9	TRUE	ALWAYS Q07.9	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 88425004

Descriptions

Relationships

Parent Concepts

Children Concepts

Extended Maps

Recent searches