Hereditary oculoleptomeningeal amyloid angiopathy 43532007
SNOMED CT code
SNOMED code | 43532007 |
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name | Hereditary oculoleptomeningeal amyloid angiopathy |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Hereditary oculoleptomeningeal amyloid angiopathy (disorder) |
synonyms |
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attributes - group1 | |
Causative agent | Prealbumin 37959007 |
Associated morphology | Amyloid deposition 68790008 |
Finding site | Leptomeninges structure 66697007 |
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 Hereditary oculoleptomeningeal amyloid angiopathy 43532007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Hereditary oculoleptomeningeal amyloid angiopathy 43532007 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Finding of meninges 299729001 Disorder of meninges 15758002 Hereditary oculoleptomeningeal amyloid angiopathy 43532007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Amyloidosis 17602002 Hereditary amyloidosis 367601000119103 Hereditary oculoleptomeningeal amyloid angiopathy 43532007 |
ancestors | sorted most to least specific
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cpt crosswalks |
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