Intellectual disability, epilepsy, extrapyramidal syndrome 1187210007
SNOMED CT code
| SNOMED code | 1187210007 |
|---|---|
| name | Intellectual disability, epilepsy, extrapyramidal syndrome |
| status | active |
| date introduced | 2021-11-30 |
| fully specified name(s) | Intellectual disability, epilepsy, extrapyramidal syndrome (disorder) |
| synonyms | Intellectual disability, epilepsy, extrapyramidal syndrome |
| attributes - group5 | |
| Interprets | Muscle tone 6918002 |
| attributes - group4 | |
| Interprets | Ability to perform function / activity 364665006 |
| Has interpretation | Impaired 260379002 |
| attributes - group1 | |
| Occurrence | Infancy 3658006 |
| Finding site | Skeletal muscle structure 127954009 |
| attributes - group2 | |
| Occurrence | Infancy 3658006 |
| Finding site | Extrapyramidal system structure 76375004 |
| attributes - group3 | |
| Occurrence | Infancy 3658006 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group6 | |
| Interprets | Intellectual ability 247573007 |
| Has interpretation | Impaired 260379002 |
| attributes - group7 | |
| 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 Intellectual disability, epilepsy, extrapyramidal syndrome 1187210007 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Seizure 91175000 Seizure disorder 128613002 Intellectual disability, epilepsy, extrapyramidal syndrome 1187210007 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Finding of functional performance and activity 248536006 Developmental disorder of motor function 268674003 Intellectual disability, epilepsy, extrapyramidal syndrome 1187210007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Intellectual disability, epilepsy, extrapyramidal syndrome 1187210007 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Intellectual disability, epilepsy, extrapyramidal syndrome 1187210007 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 Intellectual disability, epilepsy, extrapyramidal syndrome 1187210007 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Poor muscle tone 398152000 Intellectual disability, epilepsy, extrapyramidal syndrome 1187210007 SNOMED CT Concept 138875005 Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Disorder of skeletal muscle 75047002 Intellectual disability, epilepsy, extrapyramidal syndrome 1187210007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Intellectual disability, epilepsy, extrapyramidal syndrome 1187210007 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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