Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome 765089003
SNOMED CT code
SNOMED code | 765089003 |
---|---|
name | Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome |
status | active |
date introduced | 2018-07-31 |
fully specified name(s) | Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome (disorder) |
synonyms |
|
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Morphologically abnormal structure 49755003 |
Occurrence | Congenital 255399007 |
Finding site | Cerebellar structure 113305005 |
attributes - group2 | |
Interprets | Intellectual ability 247573007 |
Has interpretation | Impaired 260379002 |
attributes - group3 | |
Interprets | Adaptation behavior 406208005 |
Has interpretation | Impaired 260379002 |
parents | |
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 Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome 765089003 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Seizure 91175000 Seizure disorder 128613002 Epilepsy 84757009 Localization-related epilepsy 230381009 Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome 765089003 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Disorder of brain 81308009 Cerebellar disorder 223176004 Dysgenesis of the cerebellum 253171007 Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome 765089003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome 765089003 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 Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome 765089003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome 765089003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome 765089003 |
ancestors | sorted most to least specific
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cpt crosswalks |
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