Pelizaeus-Merzbacher disease, connatal variant 59636002
SNOMED CT code
SNOMED code | 59636002 |
---|---|
name | Pelizaeus-Merzbacher disease, connatal variant |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Pelizaeus-Merzbacher disease, connatal variant (disorder) |
synonyms |
|
attributes - group1 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Myelin sheath alteration 125495003 |
Finding site | Myelinated nerve fiber structure 54115001 |
attributes - group2 | |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Dystrophy 4720007 |
Finding site | White matter structure of brain and spinal cord 389080008 |
parents |
|
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked recessive hereditary disease 1162976004 Pelizaeus-Merzbacher disease, connatal variant 59636002 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 Congenital anomaly of central nervous system 128124001 Pelizaeus-Merzbacher disease, connatal variant 59636002 SNOMED CT Concept 138875005 Clinical finding 404684003 Neurological lesion 299735001 Leukodystrophy 192781003 Pelizaeus-Merzbacher disease 64855000 Pelizaeus-Merzbacher disease, connatal variant 59636002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Congenital degeneration of nervous system 95477007 Pelizaeus-Merzbacher disease, connatal variant 59636002 |
ancestors | sorted most to least specific
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cpt crosswalks |
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