Pachygyria, intellectual disability, epilepsy syndrome 763861000
SNOMED CT code
SNOMED code | 763861000 |
---|---|
name | Pachygyria, intellectual disability, epilepsy syndrome |
status | active |
date introduced | 2018-07-31 |
fully specified name(s) | Pachygyria, intellectual disability, epilepsy syndrome (disorder) |
synonyms |
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attributes - group2 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Arachnoid cyst 785284009 |
Occurrence | Congenital 255399007 |
Finding site | Arachnoid structure 75042008 |
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Enlargement 442021009 |
Occurrence | Congenital 255399007 |
Finding site | Cerebral gyrus 279165009 |
attributes - group3 | |
Interprets | Intellectual ability 247573007 |
Has interpretation | Impaired 260379002 |
attributes - group4 | |
Interprets | Adaptation behavior 406208005 |
Has interpretation | Impaired 260379002 |
parents |
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hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Mental state, behavior and/or psychosocial function finding 384821006 Behavior finding 844005 Intellectual disability 110359009 Pachygyria, intellectual disability, epilepsy syndrome 763861000 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Seizure 91175000 Seizure disorder 128613002 Pachygyria, intellectual disability, epilepsy syndrome 763861000 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of head and neck region 118254002 Head finding 406122000 Finding of head region 298364001 Macrogyria 23024003 Pachygyria, intellectual disability, epilepsy syndrome 763861000 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 Congenital anomaly of central nervous system 128124001 Congenital malformation of the meninges 253199003 Pachygyria, intellectual disability, epilepsy syndrome 763861000 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of meninges 299729001 Disorder of meninges 15758002 Meningeal cyst 302883007 Arachnoid cyst 33595009 Pachygyria, intellectual disability, epilepsy syndrome 763861000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Pachygyria, intellectual disability, epilepsy syndrome 763861000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Pachygyria, intellectual disability, epilepsy syndrome 763861000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Pachygyria, intellectual disability, epilepsy syndrome 763861000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Pachygyria, intellectual disability, epilepsy syndrome 763861000 |
ancestors | sorted most to least specific
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cpt crosswalks |
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