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Autosomal recessive isolated optic atrophy (disorder)
Autosomal recessive isolated optic atrophy
Autosomal recessive non-syndromic optic atrophy
A rare hereditary optic atrophy characterized by an early onset of bilateral optic nerve degeneration without other systemic features. Clinical manifestations include pallor of the optic disks, severe but slowly progressing visual impairment, and in some patients also paracentral scotoma, photophobia and dyschromatopsia.
Id1197151003
StatusPrimitive
Associated morphologyAtrophy
Finding siteStructure of left optic nerve
Associated morphologyAtrophy
Finding siteStructure of right optic nerve
ICD-10 complex map reference set
TargetH47.2
RuleTRUE
AdviceALWAYS H47.2 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified