Neurofibromatosis type 2 92503002
SNOMED CT code
SNOMED code | 92503002 |
---|---|
name | Neurofibromatosis type 2 |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Neurofibromatosis type 2 (disorder) |
synonyms |
|
attributes - group2 | |
Associated morphology | Neurofibromatosis 81669005 |
Occurrence | Congenital 255399007 |
Finding site | Nervous system structure 25087005 |
attributes - group3 | |
Associated morphology | Neurofibromatosis 81669005 |
Occurrence | Congenital 255399007 |
Finding site | Skin structure 39937001 |
attributes - group1 | |
Finding site | Vestibulocochlear nerve structure 8598002 |
Associated morphology | Schwannoma 985004 |
parents |
|
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Neurocutaneous syndrome 78572006 Neurofibromatosis syndrome 19133005 Neurofibromatosis type 2 92503002 SNOMED CT Concept 138875005 Clinical finding 404684003 Neurological lesion 299735001 Space-occupying lesion of nervous system 281229000 Neoplasm of nervous system 126950007 Neoplasm of cranial nerve 126966009 Benign neoplasm of cranial nerve 92071005 Schwannoma of cranial nerve 629149351000119106 Neurofibromatosis type 2 92503002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Neurofibromatosis type 2 92503002 SNOMED CT Concept 138875005 Clinical finding 404684003 Neurological lesion 299735001 Lesion of the acoustic nerve 95829004 Neoplasm of vestibulocochlear nerve 387891008 Benign neoplasm of vestibulocochlear nerve 91962001 Neurofibromatosis type 2 92503002 |
ancestors | sorted most to least specific
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cpt crosswalks |
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