Granular cell hypoplasia 253178001
SNOMED CT code
SNOMED code | 253178001 |
---|---|
name | Granular cell hypoplasia |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Granular cell hypoplasia (disorder) |
synonyms | Granular cell hypoplasia |
attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Hypoplasia 55199003 |
Occurrence | Congenital 255399007 |
Finding site | Cerebellar cortex structure 25991003 |
parents | Congenital cerebellar hypoplasia 16026008 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Central nervous system finding 246556002 Finding of brain 299718000 Disorder of brain 81308009 Cerebellar disorder 223176004 Dysgenesis of the cerebellum 253171007 Congenital cerebellar hypoplasia 16026008 Granular cell hypoplasia 253178001 |
ancestors | sorted most to least specific
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cpt crosswalks |
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