Diagnosis Code: H47.22

Short Description: Hereditary optic atrophy

Long Description: Hereditary optic atrophy

The code H47.22 is VALID for claim submission

Code Classification:

• Diseases of the eye and adnexa (H00–H59)
  • Disorders of optic nerve and visual pathways (H46-H47)
    • Other disorders of optic [2nd] nerve and visual pathways (H47)
      • H47.22 Hereditary optic atrophy

Code Version: 2022 ICD-10-CM

Synonyms

• Absence of teeth
• Auditory neuropathy, optic atrophy syndrome
• Autosomal dominant optic atrophy and cataract
• Autosomal dominant optic atrophy and peripheral neuropathy syndrome
• Autosomal dominant optic atrophy classic form
• Autosomal dominant optic atrophy plus syndrome
• Autosomal recessive bilateral optic atrophy
• Autosomal recessive isolated optic atrophy
• Autosomal recessive optic atrophy type 6
• Autosomal recessive optic atrophy type 7
• Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome
• Axonal neuropathy
• Bilateral optic atrophy of eyes
• Bilateral optic atrophy of eyes
• Bilateral optic atrophy of eyes
• Bilateral primary optic atrophy
• Bilateral primary optic atrophy
• CAMOS syndrome
• Cerebellar ataxia, areflexia, pes cavus, optic atrophy, sensorineural hearing loss syndrome
• Childhood-onset autosomal dominant optic atrophy
• Congenital atrophy of optic nerve
• Congenital atrophy of optic nerve
• Congenital atrophy of optic nerve
• Congenital atrophy of optic nerve
• Congenital atrophy of optic nerve
• Dominant hereditary optic atrophy
• Dominant hereditary optic atrophy
• Dominant hereditary optic atrophy
• Dominant hereditary optic atrophy
• Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome
• Early-onset X-linked optic atrophy
• False anodontia
• GAPO syndrome
• Generalized dystonia
• Genetic anomaly of leukocyte
• Hereditary bilateral optic atrophy
• Hereditary left optic atrophy
• Hereditary motor and sensory neuropathy with optic atrophy
• Hereditary optic atrophy
• Hereditary right optic atrophy
• Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome
• Leber plus disease
• Leber's optic atrophy
• Maternally inherited mitochondrial deoxyribonucleic acid disease
• Maternally inherited mitochondrial deoxyribonucleic acid disease
• MEPAN syndrome
• Optic atrophy, ataxia, peripheral neuropathy, global developmental delay syndrome
• Optic atrophy, intellectual disability syndrome
• Pelger-Huët anomaly
• Pelger-Huët cell
• Second cranial nerve finding
• Second cranial nerve finding
• Second cranial nerve finding
• Second cranial nerve finding
• Severe X-linked intellectual disability Gustavson type
• Short stature, optic nerve atrophy, Pelger-Huët anomaly syndrome
• Spastic paraplegia, optic atrophy, neuropathy syndrome
• SPOAN and SPOAN-related disorder
• SPOAN and SPOAN-related disorder
• Tooth absent
• X-linked optic atrophy

References to Index of Diseases and Injuries

The code H47.22 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Leber's optic atrophy

Crosswalk Information

Similar Codes

This page was last updated on: 10/1/2023

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