X-linked spasticity, intellectual disability, epilepsy syndrome 725163002
SNOMED CT code
| SNOMED code | 725163002 |
|---|---|
| name | X-linked spasticity, intellectual disability, epilepsy syndrome |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | X-linked spasticity, intellectual disability, epilepsy syndrome (disorder) |
| synonyms | X-linked spasticity, intellectual disability, epilepsy syndrome |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Brain structure 12738006 |
| attributes - group5 | |
| Interprets | Intellectual ability 247573007 |
| Has interpretation | Impaired 260379002 |
| attributes - group6 | |
| Interprets | Adaptation behavior 406208005 |
| Has interpretation | Impaired 260379002 |
| attributes - group2 | |
| Finding site | Cerebrum 83678007 |
| attributes - group3 | |
| Finding site | Skeletal muscle structure 127954009 |
| attributes - group4 | |
| Has interpretation | Increased 35105006 |
| Interprets | Muscle tone 6918002 |
| 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 X-linked spasticity, intellectual disability, epilepsy syndrome 725163002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked recessive hereditary disease 1162976004 X-linked spasticity, intellectual disability, epilepsy syndrome 725163002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Neurodevelopmental disorder 700364009 Developmental and epileptic encephalopathy 1275631007 Myoclonic encephalopathy 192845009 X-linked spasticity, intellectual disability, epilepsy syndrome 725163002 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Spasticity 221360009 X-linked spasticity, intellectual disability, epilepsy syndrome 725163002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 X-linked spasticity, intellectual disability, epilepsy syndrome 725163002 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 X-linked spasticity, intellectual disability, epilepsy syndrome 725163002 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 X-linked spasticity, intellectual disability, epilepsy syndrome 725163002 SNOMED CT Concept 138875005 Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Disorder of skeletal muscle 75047002 X-linked spasticity, intellectual disability, epilepsy syndrome 725163002 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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