Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome 442511009
SNOMED CT code
| SNOMED code | 442511009 |
|---|---|
| name | Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome |
| status | active |
| date introduced | 2009-07-31 |
| fully specified name(s) | Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome (disorder) |
| synonyms |
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| attributes - group1 | |
| Associated morphology | Degenerative abnormality 107669003 |
| Finding site | Brain structure 12738006 |
| attributes - group2 | |
| Finding site | Limb structure 66019005 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Lymphatic edema 30213001 |
| attributes - group3 | |
| Clinical course | Progressive 255314001 |
| attributes - group4 | |
| Finding site | Optic nerve structure 18234004 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disease of the central nervous system 80690008 Hereditary degenerative disease of central nervous system 106018006 Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome 442511009 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Second cranial nerve finding 106152006 Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome 442511009 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Seizure 91175000 Seizure disorder 128613002 Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome 442511009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome 442511009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Primary lymphedema 1217009002 Hereditary lymphedema 254199006 Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome 442511009 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Inherited optic neuropathy 312942003 Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome 442511009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disease of the central nervous system 80690008 Degenerative brain disorder 52522001 Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome 442511009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Chronic disease 27624003 Chronic nervous system disorder 128283000 Chronic brain syndrome 78689005 Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome 442511009 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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