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  2. ICD-10-CM Codes
  3. H00–H59
  4. H46-H47
  5. Other disorders of optic [2nd] nerve and visual pathways (H47)

Other disorders of optic [2nd] nerve and visual pathways (H47)

    • ICD-10 Index

      • 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 - Other disorders of optic [2nd] nerve and visual pathways NON-BILLABLE CODE
            • H47.0 - Disorders of optic nerve, not elsewhere classified NON-BILLABLE CODE
            • H47.01 - Ischemic optic neuropathy NON-BILLABLE CODE
            • H47.011 - Ischemic optic neuropathy, right eye BILLABLE CODE
            • H47.012 - Ischemic optic neuropathy, left eye BILLABLE CODE
            • H47.013 - Ischemic optic neuropathy, bilateral BILLABLE CODE
            • H47.019 - Ischemic optic neuropathy, unspecified eye BILLABLE CODE
            • H47.02 - Hemorrhage in optic nerve sheath NON-BILLABLE CODE
            • H47.021 - Hemorrhage in optic nerve sheath, right eye BILLABLE CODE
            • H47.022 - Hemorrhage in optic nerve sheath, left eye BILLABLE CODE
            • H47.023 - Hemorrhage in optic nerve sheath, bilateral BILLABLE CODE
            • H47.029 - Hemorrhage in optic nerve sheath, unspecified eye BILLABLE CODE
            • H47.03 - Optic nerve hypoplasia NON-BILLABLE CODE
            • H47.031 - Optic nerve hypoplasia, right eye BILLABLE CODE
            • H47.032 - Optic nerve hypoplasia, left eye BILLABLE CODE
            • H47.033 - Optic nerve hypoplasia, bilateral BILLABLE CODE
            • H47.039 - Optic nerve hypoplasia, unspecified eye BILLABLE CODE
            • H47.09 - Other disorders of optic nerve, not elsewhere classified NON-BILLABLE CODE
            • H47.091 - Oth disorders of optic nerve, NEC, right eye BILLABLE CODE
            • H47.092 - Oth disorders of optic nerve, NEC, left eye BILLABLE CODE
            • H47.093 - Oth disorders of optic nerve, NEC, bilateral BILLABLE CODE
            • H47.099 - Oth disorders of optic nerve, NEC, unsp eye BILLABLE CODE
            • H47.1 - Papilledema NON-BILLABLE CODE
            • H47.10 - Unspecified papilledema BILLABLE CODE
            • H47.11 - Papilledema associated with increased intracranial pressure BILLABLE CODE
            • H47.12 - Papilledema associated with decreased ocular pressure BILLABLE CODE
            • H47.13 - Papilledema associated with retinal disorder BILLABLE CODE
            • H47.14 - Foster-Kennedy syndrome NON-BILLABLE CODE
            • H47.141 - Foster-Kennedy syndrome, right eye BILLABLE CODE
            • H47.142 - Foster-Kennedy syndrome, left eye BILLABLE CODE
            • H47.143 - Foster-Kennedy syndrome, bilateral BILLABLE CODE
            • H47.149 - Foster-Kennedy syndrome, unspecified eye BILLABLE CODE
            • H47.2 - Optic atrophy NON-BILLABLE CODE
            • H47.20 - Unspecified optic atrophy BILLABLE CODE
            • H47.21 - Primary optic atrophy NON-BILLABLE CODE
            • H47.211 - Primary optic atrophy, right eye BILLABLE CODE
            • H47.212 - Primary optic atrophy, left eye BILLABLE CODE
            • H47.213 - Primary optic atrophy, bilateral BILLABLE CODE
            • H47.219 - Primary optic atrophy, unspecified eye BILLABLE CODE
            • H47.22 - Hereditary optic atrophy BILLABLE CODE
            • H47.23 - Glaucomatous optic atrophy NON-BILLABLE CODE
            • H47.231 - Glaucomatous optic atrophy, right eye BILLABLE CODE
            • H47.232 - Glaucomatous optic atrophy, left eye BILLABLE CODE
            • H47.233 - Glaucomatous optic atrophy, bilateral BILLABLE CODE
            • H47.239 - Glaucomatous optic atrophy, unspecified eye BILLABLE CODE
            • H47.29 - Other optic atrophy NON-BILLABLE CODE
            • H47.291 - Other optic atrophy, right eye BILLABLE CODE
            • H47.292 - Other optic atrophy, left eye BILLABLE CODE
            • H47.293 - Other optic atrophy, bilateral BILLABLE CODE
            • H47.299 - Other optic atrophy, unspecified eye BILLABLE CODE
            • H47.3 - Other disorders of optic disc NON-BILLABLE CODE
            • H47.31 - Coloboma of optic disc NON-BILLABLE CODE
            • H47.311 - Coloboma of optic disc, right eye BILLABLE CODE
            • H47.312 - Coloboma of optic disc, left eye BILLABLE CODE
            • H47.313 - Coloboma of optic disc, bilateral BILLABLE CODE
            • H47.319 - Coloboma of optic disc, unspecified eye BILLABLE CODE
            • H47.32 - Drusen of optic disc NON-BILLABLE CODE
            • H47.321 - Drusen of optic disc, right eye BILLABLE CODE
            • H47.322 - Drusen of optic disc, left eye BILLABLE CODE
            • H47.323 - Drusen of optic disc, bilateral BILLABLE CODE
            • H47.329 - Drusen of optic disc, unspecified eye BILLABLE CODE
            • H47.33 - Pseudopapilledema of optic disc NON-BILLABLE CODE
            • H47.331 - Pseudopapilledema of optic disc, right eye BILLABLE CODE
            • H47.332 - Pseudopapilledema of optic disc, left eye BILLABLE CODE
            • H47.333 - Pseudopapilledema of optic disc, bilateral BILLABLE CODE
            • H47.339 - Pseudopapilledema of optic disc, unspecified eye BILLABLE CODE
            • H47.39 - Other disorders of optic disc NON-BILLABLE CODE
            • H47.391 - Other disorders of optic disc, right eye BILLABLE CODE
            • H47.392 - Other disorders of optic disc, left eye BILLABLE CODE
            • H47.393 - Other disorders of optic disc, bilateral BILLABLE CODE
            • H47.399 - Other disorders of optic disc, unspecified eye BILLABLE CODE
            • H47.4 - Disorders of optic chiasm NON-BILLABLE CODE
            • H47.41 - Disorders of optic chiasm in (due to) inflammatory disorders BILLABLE CODE
            • H47.42 - Disorders of optic chiasm in (due to) neoplasm BILLABLE CODE
            • H47.43 - Disorders of optic chiasm in (due to) vascular disorders BILLABLE CODE
            • H47.49 - Disorders of optic chiasm in (due to) other disorders BILLABLE CODE
            • H47.5 - Disorders of other visual pathways NON-BILLABLE CODE
            • H47.51 - Disorders of visual pathways in (due to) inflam disorders NON-BILLABLE CODE
            • H47.511 - Disord of visual pathways in inflam disord, right side BILLABLE CODE
            • H47.512 - Disord of visual pathways in inflam disord, left side BILLABLE CODE
            • H47.519 - Disord of visual pathways in inflam disord, unsp side BILLABLE CODE
            • H47.52 - Disorders of visual pathways in (due to) neoplasm NON-BILLABLE CODE
            • H47.521 - Disord of visual pathways in (due to) neoplasm, right side BILLABLE CODE
            • H47.522 - Disorders of visual pathways in (due to) neoplasm, left side BILLABLE CODE
            • H47.529 - Disorders of visual pathways in (due to) neoplasm, unsp side BILLABLE CODE
            • H47.53 - Disorders of visual pathways in (due to) vascular disorders NON-BILLABLE CODE
            • H47.531 - Disord of visual pathways in vascular disord, right side BILLABLE CODE
            • H47.532 - Disord of visual pathways in vascular disord, left side BILLABLE CODE
            • H47.539 - Disord of visual pathways in vascular disord, unsp side BILLABLE CODE
            • H47.6 - Disorders of visual cortex NON-BILLABLE CODE
            • H47.61 - Cortical blindness NON-BILLABLE CODE
            • H47.611 - Cortical blindness, right side of brain BILLABLE CODE
            • H47.612 - Cortical blindness, left side of brain BILLABLE CODE
            • H47.619 - Cortical blindness, unspecified side of brain BILLABLE CODE
            • H47.62 - Disorders of visual cortex in (due to) inflam disorders NON-BILLABLE CODE
            • H47.621 - Disord of visual cortex in inflam disord, r side of brain BILLABLE CODE
            • H47.622 - Disord of visual cortex in inflam disord, left side of brain BILLABLE CODE
            • H47.629 - Disord of visual cortex in inflam disord, unsp side of brain BILLABLE CODE
            • H47.63 - Disorders of visual cortex in (due to) neoplasm NON-BILLABLE CODE
            • H47.631 - Disord of visual cortex in neoplasm, right side of brain BILLABLE CODE
            • H47.632 - Disord of visual cortex in neoplasm, left side of brain BILLABLE CODE
            • H47.639 - Disord of visual cortex in neoplasm, unsp side of brain BILLABLE CODE
            • H47.64 - Disorders of visual cortex in (due to) vascular disorders NON-BILLABLE CODE
            • H47.641 - Disord of visual cortex in vasc disord, right side of brain BILLABLE CODE
            • H47.642 - Disord of visual cortex in vasc disord, left side of brain BILLABLE CODE
            • H47.649 - Disord of visual cortex in vasc disord, unsp side of brain BILLABLE CODE
            • H47.9 - Unspecified disorder of visual pathways BILLABLE CODE

Clinical Information for Other disorders of optic [2nd] nerve and visual pathways (H47)

Optic Atrophy - Atrophy of the optic disk which may be congenital or acquired. This condition indicates a deficiency in the number of nerve fibers which arise in the RETINA and converge to form the OPTIC DISK; OPTIC NERVE; OPTIC CHIASM; and optic tracts. GLAUCOMA; ISCHEMIA; inflammation, a chronic elevation of intracranial pressure, toxins, optic nerve compression, and inherited conditions (see OPTIC ATROPHIES, HEREDITARY) are relatively common causes of this condition.

Optic Atrophy, Autosomal Dominant - Dominant optic atrophy is a hereditary optic neuropathy causing decreased visual acuity, color vision deficits, a centrocecal scotoma, and optic nerve pallor (Hum. Genet. 1998; 102: 79-86). Mutations leading to this condition have been mapped to the OPA1 gene at chromosome 3q28-q29. OPA1 codes for a dynamin-related GTPase that localizes to mitochondria.

Optic Atrophy, Hereditary, Leber - A maternally linked genetic disorder that presents in mid-life as acute or subacute central vision loss leading to central scotoma and blindness. The disease has been associated with missense mutations in the mtDNA, in genes for Complex I, III, and IV polypeptides, that can act autonomously or in association with each other to cause the disease. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim/, MIM#535000 (April 17, 2001))

Optic Nerve Hypoplasia - A group of rare genetic disorders characterized by underdeveloped OPTIC NERVES, resulting in increased incidences of vision impairment, CONGENITAL NYSTAGMUS and STRABISMUS. It may be syndromic, and is often associated with CNS malformations.

Optic Atrophies, Hereditary - Hereditary conditions that feature progressive visual loss in association with optic atrophy. Relatively common forms include autosomal dominant optic atrophy (OPTIC ATROPHY, AUTOSOMAL DOMINANT) and Leber hereditary optic atrophy (OPTIC ATROPHY, HEREDITARY, LEBER).

Papilledema - Swelling of the OPTIC DISK, usually in association with increased intracranial pressure, characterized by hyperemia, blurring of the disk margins, microhemorrhages, blind spot enlargement, and engorgement of retinal veins. Chronic papilledema may cause OPTIC ATROPHY and visual loss. (Miller et al., Clinical Neuro-Ophthalmology, 4th ed, p175)

Optic Atrophies, Hereditary - Hereditary conditions that feature progressive visual loss in association with optic atrophy. Relatively common forms include autosomal dominant optic atrophy (OPTIC ATROPHY, AUTOSOMAL DOMINANT) and Leber hereditary optic atrophy (OPTIC ATROPHY, HEREDITARY, LEBER).

Optic Atrophy - Atrophy of the optic disk which may be congenital or acquired. This condition indicates a deficiency in the number of nerve fibers which arise in the RETINA and converge to form the OPTIC DISK; OPTIC NERVE; OPTIC CHIASM; and optic tracts. GLAUCOMA; ISCHEMIA; inflammation, a chronic elevation of intracranial pressure, toxins, optic nerve compression, and inherited conditions (see OPTIC ATROPHIES, HEREDITARY) are relatively common causes of this condition.

Optic Atrophy, Autosomal Dominant - Dominant optic atrophy is a hereditary optic neuropathy causing decreased visual acuity, color vision deficits, a centrocecal scotoma, and optic nerve pallor (Hum. Genet. 1998; 102: 79-86). Mutations leading to this condition have been mapped to the OPA1 gene at chromosome 3q28-q29. OPA1 codes for a dynamin-related GTPase that localizes to mitochondria.

Optic Atrophies, Hereditary - Hereditary conditions that feature progressive visual loss in association with optic atrophy. Relatively common forms include autosomal dominant optic atrophy (OPTIC ATROPHY, AUTOSOMAL DOMINANT) and Leber hereditary optic atrophy (OPTIC ATROPHY, HEREDITARY, LEBER).

Optic Atrophy - Atrophy of the optic disk which may be congenital or acquired. This condition indicates a deficiency in the number of nerve fibers which arise in the RETINA and converge to form the OPTIC DISK; OPTIC NERVE; OPTIC CHIASM; and optic tracts. GLAUCOMA; ISCHEMIA; inflammation, a chronic elevation of intracranial pressure, toxins, optic nerve compression, and inherited conditions (see OPTIC ATROPHIES, HEREDITARY) are relatively common causes of this condition.

Optic Atrophy, Autosomal Dominant - Dominant optic atrophy is a hereditary optic neuropathy causing decreased visual acuity, color vision deficits, a centrocecal scotoma, and optic nerve pallor (Hum. Genet. 1998; 102: 79-86). Mutations leading to this condition have been mapped to the OPA1 gene at chromosome 3q28-q29. OPA1 codes for a dynamin-related GTPase that localizes to mitochondria.

Optic Atrophy, Hereditary, Leber - A maternally linked genetic disorder that presents in mid-life as acute or subacute central vision loss leading to central scotoma and blindness. The disease has been associated with missense mutations in the mtDNA, in genes for Complex I, III, and IV polypeptides, that can act autonomously or in association with each other to cause the disease. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim/, MIM#535000 (April 17, 2001))

Optic Atrophy, Hereditary, Leber - A maternally linked genetic disorder that presents in mid-life as acute or subacute central vision loss leading to central scotoma and blindness. The disease has been associated with missense mutations in the mtDNA, in genes for Complex I, III, and IV polypeptides, that can act autonomously or in association with each other to cause the disease. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim/, MIM#535000 (April 17, 2001))

Papilledema - Swelling of the OPTIC DISK, usually in association with increased intracranial pressure, characterized by hyperemia, blurring of the disk margins, microhemorrhages, blind spot enlargement, and engorgement of retinal veins. Chronic papilledema may cause OPTIC ATROPHY and visual loss. (Miller et al., Clinical Neuro-Ophthalmology, 4th ed, p175)