Autosomal dominant hereditary disorder
Hereditary optic atrophy
||
Childhood-onset autosomal dominant optic atrophy (disorder)
Childhood-onset autosomal dominant optic atrophy
autosomaal dominante opticusatrofie beginnend op kinderleeftijd
autosomaal dominante atrofie van nervus opticus beginnend op kinderleeftijd
Id838307002
StatusPrimitive
Associated morphologyPrimary atrophy
Finding siteOptic nerve structure
OccurrenceChildhood
ICD-10 complex map reference set
TargetH47.2
RuleTRUE
AdviceALWAYS H47.2
CorrelationSNOMED CT source code to target map code correlation not specified