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Terminology chevron_right Concepts chevron_right 128613002

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Component

128613002

The component that hold information about this concept.

Fully Specified Name (FSN)

Seizure disorder (disorder)

Shortest Term

Bệnh co giật

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

Seizure disorder (disorder)

SCTID: 128613002, Defined, Active

128613002|Seizure disorder (disorder)|

vi Bệnh co giật
en Seizure disorder
en Seizure disorder (disorder)

Expression

128613002 |Seizure disorder (disorder)|
 === 81308009 |Disorder of brain (disorder)| + 
91175000 |Seizure (finding)| : 
        { 363698007 |Finding site (attribute)| = 12738006 |Brain structure (body structure)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
593661000003116 - bệnh co giật (vi) View
593661000003116	vi	Synonym (core metadata concept)	bệnh co giật	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
206998011 - Seizure disorder (en) View
206998011	en	Synonym (core metadata concept)	Seizure disorder	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True
732627018 - Seizure disorder (disorder) (en) View
732627018	en	Fully specified name (core metadata concept)	Seizure disorder (disorder)	900000000000448009 \|Entire term case insensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (698124027) - 128613002 -> 12738006 (363698007) View
363698007 \|Finding site (attribute)\|	12738006 \|Brain structure (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2264206023) - 128613002 -> 91175000 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	91175000 \|Seizure (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (9181425022) - 128613002 -> 91175000 (116680003) View
116680003 \|Is a (attribute)\|	91175000 \|Seizure (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (164012025) - 128613002 -> 81308009 (116680003) View
116680003 \|Is a (attribute)\|	81308009 \|Disorder of brain (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
81308009 View
81308009	Disorder of brain (disorder)	Encephalopathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
91175000 View
91175000	Seizure (finding)	Fit	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
191714002 View
191714002	Dissociative convulsions (disorder)	Sham seizures	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1351854006 View
1351854006	Primary hypomagnesemia, generalized seizures, intellectual disability, obesity syndrome (disorder)	Primary hypomagnesemia, generalized seizures, intellectual disability, obesity syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1303273003 View
1303273003	Interferon regulatory factor 2 binding protein like-related regressive neurodevelopmental disorder, dystonia, seizures syndrome (disorder)	Irf2bpl-related regressive neurodevelopmental disorder, dystonia, seizures syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1269236003 View
1269236003	Primary hypomagnesemia, refractory seizures, intellectual disability syndrome (disorder)	Primary hypomagnesemia, refractory seizures, intellectual disability syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1254960008 View
1254960008	Seizure co-occurrent and due to substance withdrawal (disorder)	Seizure co-occurrent and due to substance withdrawal	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1217381009 View
1217381009	Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome (disorder)	Gpaa1-related biosynthesis defect	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1208747005 View
1208747005	Inosine triphosphate pyrophosphohydrolase-related lethal infantile neurological disorder with cataract and cardiac involvement (disorder)	Martsolf-like syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
230432008 View
230432008	Familial febrile convulsions (disorder)	Familial febrile convulsions	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
1187304005 View
1187304005	Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome (disorder)	Minds syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1187210007 View
1187210007	Intellectual disability, epilepsy, extrapyramidal syndrome (disorder)	Intellectual disability, epilepsy, extrapyramidal syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1187250005 View
1187250005	Seizures, scoliosis, macrocephaly syndrome (disorder)	Seizures, scoliosis, macrocephaly syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
1172630000 View
1172630000	Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome (disorder)	Global developmental delay, neuro-ophthalmological abnormalities, seizures, intellectual disability syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
789063000 View
789063000	Primary hyperaldosteronism, seizures, neurological abnormalities syndrome (disorder)	Primary hyperaldosteronism, seizures, neurological abnormalities syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
785303004 View
785303004	Multiple congenital anomalies, hypotonia, seizures syndrome (disorder)	Multiple congenital anomalies, hypotonia, seizures syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
770678005 View
770678005	Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome (disorder)	Peho-like syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
770755007 View
770755007	Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome (disorder)	Congenital disorder of glycosylation due to pigt deficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
770758009 View
770758009	New-onset refractory status epilepticus (disorder)	New-onset refractory status epilepticus	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
763861000 View
763861000	Pachygyria, intellectual disability, epilepsy syndrome (disorder)	Kuzniecky syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
768473009 View
768473009	Purine rich element binding protein a syndrome (disorder)	Pura syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
768555009 View
768555009	5q31.3 microdeletion syndrome (disorder)	5q31.3 microdeletion syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
723304001 View
723304001	Microcephaly, seizure, intellectual disability, heart disease syndrome (disorder)	Microcephaly, seizure, intellectual disability, heart disease syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
719810000 View
719810000	X-linked intellectual disability with seizure and psoriasis syndrome (disorder)	Tranebjaerg svejgaard syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
720010009 View
720010009	Microphthalmia with brain atrophy syndrome (disorder)	Moba syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
721207002 View
721207002	Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome (disorder)	Sesame syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
722110003 View
722110003	Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome (disorder)	Al gazali nair syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
722762005 View
722762005	Ganglioside gm3 synthase deficiency (disorder)	Gm3 synthase deficiency	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
702344008 View
702344008	Pitt-hopkins syndrome (disorder)	Pitt-hopkins syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
137991000119103 View
137991000119103	Seizure disorder as sequela of stroke (disorder)	Seizure disorder as sequela of stroke	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
442511009 View
442511009	Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome (disorder)	Peho syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
371107004 View
371107004	Seizures complicating intracranial hemorrhage in the newborn (disorder)	Seizures complicating intracranial hemorrhage in the newborn	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
371022006 View
371022006	Seizures due to metabolic disorder (disorder)	Seizures due to metabolic disorder	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
15938005 View
15938005	Eclampsia (disorder)	Eclampsia	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
68761002 View
68761002	Epileptic vertigo (disorder)	Epileptic vertigo	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
80651009 View
80651009	Aicardi's syndrome (disorder)	Aicardi syndrome	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
84757009 View
84757009	Epilepsy (disorder)	Epilepsy	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
230431001 View
230431001	Situation-related seizures (disorder)	Situation-related seizures	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 (56f6a10d-5c02-51fe-a74e-52e984fbfda9) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	R56.8	TRUE	ALWAYS R56.8	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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