Spastic paraplegia, severe developmental delay, epilepsy syndrome 1187278006
SNOMED CT code
| SNOMED code | 1187278006 |
|---|---|
| name | Spastic paraplegia, severe developmental delay, epilepsy syndrome |
| status | active |
| date introduced | 2022-01-31 |
| fully specified name(s) | Spastic paraplegia, severe developmental delay, epilepsy syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Clinical course | Progressive 255314001 |
| attributes - group2 | |
| Finding site | Cerebrum 83678007 |
| attributes - group3 | |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group4 | |
| Finding site | Spinal cord structure 2748008 |
| Associated morphology | Degenerative abnormality 107669003 |
| attributes - group6 | |
| Interprets | Intellectual ability 247573007 |
| Has interpretation | Impaired 260379002 |
| attributes - group7 | |
| Interprets | Adaptation behavior 406208005 |
| Has interpretation | Impaired 260379002 |
| attributes - group8 | |
| Interprets | Movement 255324009 |
| attributes - group5 | |
| Finding site | Right lower extremity structure 62175007 |
| attributes - group10 | |
| Interprets | Movement observable 363847004 |
| Has interpretation | Absent 2667000 |
| attributes - group9 | |
| Finding site | Left lower extremity structure 32153003 |
| 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 Spastic paraplegia, severe developmental delay, epilepsy syndrome 1187278006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Autosomal recessive hereditary spastic paraplegia 1187279003 Spastic paraplegia, severe developmental delay, epilepsy syndrome 1187278006 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 Spastic syndrome 386781001 Spastic paraplegia 192967009 Hereditary spastic paraplegia 39912006 Complicated hereditary spastic paraplegia 230261006 Spastic paraplegia, severe developmental delay, epilepsy syndrome 1187278006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental delay 248290002 Spastic paraplegia, severe developmental delay, epilepsy syndrome 1187278006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Spastic paraplegia, severe developmental delay, epilepsy syndrome 1187278006 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of spinal cord 299733008 Myelopathy 48522003 Encephalomyelopathy 370502006 Spastic paraplegia, severe developmental delay, epilepsy syndrome 1187278006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic nervous system disorder 128283000 Chronic brain syndrome 78689005 Spastic paraplegia, severe developmental delay, epilepsy syndrome 1187278006 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Seizure 91175000 Seizure disorder 128613002 Epilepsy 84757009 Spastic paraplegia, severe developmental delay, epilepsy syndrome 1187278006 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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