H35.89

Billable

Other specified retinal disorders

Other specified retinal disorders

Status

Billable / Specific

Block

H30-H36

Parent Code

H35.8

Coding Notes

Related Codes(2)
Also Known As / Clinical Terms(479)

SNOMED CT

Clinical Terms

  • DSM (dome shaped macula) of right eye
  • Epiretinal snowbanking
  • Dome-shaped maculopathy of left eye
  • Left Purtscher retinopathy
  • Patterned macular change
  • Disorder of retina of left eye caused by pentosan polysulfate
  • Punctate retinal deposits
  • Bilateral absence of foveal reflexes
  • Purtscher retinopathy
  • Sudden acquired retinal degeneration
  • Generalized retinal degeneration
  • Retinal thickening
  • Dome-shaped maculopathy of right eye
  • Defect of nerve fiber layer of both retinas
  • ARN - Acute retinal necrosis
  • Atrophy of fundus of eye
  • Estrogen antagonist adverse reaction
  • Oestrogen antagonist adverse reaction
  • Retinal deposits of right eye
  • Purtscher retinopathy of bilateral eyes
  • Aminoquinoline antimalarial adverse reaction
  • Retinal pigment deposits
  • Retinal vitelliform deposits
  • Subretinal lesion
  • Perifoveal capillary nonperfusion of right eye
  • Bilateral Purtscher retinopathy
  • Cystic retinal tuft
  • Retinal flecking
  • Generalised progressive retinal atrophy
  • BARN - Bilateral acute retinal necrosis
  • Congenital anomaly of bilateral optic discs
  • Generalized degeneration of retina of bilateral eyes
  • RPE atrophy
  • Retinopathy of left eye caused by hydroxychloroquine
  • Right diffuse subretinal fibrosis
  • Atrophy of macula lutea
  • VSR - Venous stasis retinopathy
  • Right Purtscher retinopathy
  • RPE hyperplasia
  • Retinal nerve fiber bundle defect of right eye
  • Nerve fiber bundle defect
  • Acute macular neuroretinopathy
  • Congenital anomaly of bilateral retinas
  • Macular halo syndrome
  • Disorder of retina caused by talc
  • Stasis retinopathy
  • Tamoxifen adverse reaction
  • Hydrochloroquine retinopathy
  • Autoimmune retinopathy
  • Perifoveal capillary nonperfusion of bilateral eyes
  • Retinal nerve fibre bundle deficiency
  • Left retinopathy caused by pentosan polysulfate
  • Retinopathy of right eye caused by tamoxifen
  • Congenital coloboma of both optic discs
  • Angiomatosis of retina
  • Subretinal disciform lesion
  • Retinal deposits of both eyes
  • Bilateral defect of nerve fibre layer of retinas
  • RPE abnormality
  • Adverse reaction to tamoxifen
  • Bilateral vascular occlusion of retina of eyes
  • Defect of nerve fibre layer of left retina
  • Vascular occlusion of retina of both eyes
  • Generalized progressive retinal atrophy
  • Retinal pigment epithelial hyperplasia
  • Bilateral dome-shaped maculopathy
  • Left foveal reflex absent
  • Retinal deposits of bilateral eyes
  • Hard exudates
  • Generalized retinal degeneration of right eye
  • Bilateral retinopathy caused by pentosan polysulfate
  • Diffuse subretinal fibrosis of left eye
  • Glaucomatous retinal degeneration
  • Purtscher's retinopathy
  • Macular vitelliform deposits
  • Subretinal exudate
  • Colobomatous optic disc, macular atrophy, chorioretinopathy syndrome
  • Retinal nerve fibre bundle defect of right eye
  • Purtscher retinopathy of left eye
  • Abnormal rod or cone threshold
  • Hydroxychloroquine retinopathy
  • Macular star
  • Congenital anomaly of both optic discs
  • Retinal nerve fibre bundle defect of bilateral eyes
  • Retinopathy of right eye caused by hydroxychloroquine
  • Noncystic vitreoretinal tuft
  • Disorder of retina of bilateral eyes caused by pentosan polysulfate
  • Bilateral congenital coloboma of optic discs
  • Cherry red spot
  • Exudate of macula
  • Chorioretinal vascular disorder
  • Retinal deposits of left eye
  • RPE hypertrophy
  • Foveal reflex absent in both eyes
  • Traumatic retinopathy
  • Necrotizing herpetic retinopathy
  • Congenital coloboma of left optic disc
  • Tamoxifen retinopathy
  • Foveal reflex absent in bilateral eyes
  • AAOR - acute annular outer retinopathy
  • DSM (dome shaped macula) of bilateral eyes
  • Left diffuse subretinal fibrosis
  • Noncystic retinal tuft
  • Peripheral preretinal gliosis
  • Disorder of retina of right eye caused by pentosan polysulfate
  • Generalized degeneration of retina of right eye
  • Photoreceptor degeneration
  • Tay's sign
  • Absent foveal reflex
  • Peripheral cystic retinal tuft
  • Retinopathy of left eye caused by talc
  • Retinopathy of right eye caused by talc
  • Macular halo
  • Dome-shaped maculopathy
  • Infiltration of retina
  • Hamartoma of retina
  • Perifoveal capillary nonperfusion
  • Perifoveal capillary nonperfusion of left eye
  • Generalised retinal degeneration
  • Dome-shaped maculopathy of bilateral eyes
  • Hard retinal exudates
  • Disorder of retina caused by pentosan polysulfate
  • Zonular traction vitreoretinal tuft
  • Bilateral retinal hamartoma
  • Defect of nerve fibre layer of bilateral retinas
  • Subretinal fibrosis
  • Cystic vitreoretinal tuft
  • Hamartoma of retina of bilateral eyes
  • Macular exudate
  • Congenital anomaly of right optic disc
  • Crystals in the retina
  • Retinal nerve fiber bundle defect of bilateral eyes
  • Radiation retinopathy
  • Diffuse subretinal fibrosis of both eyes
  • Valsalva retinopathy
  • Toxic retinopathy
  • Defect of nerve fibre layer of both retinas
  • Slow flow retinopathy
  • Perifoveal capillary nonperfusion of both eyes
  • Retinal atrophy
  • Reticular pseudodrusen
  • Generalized retinal degeneration of left eye
  • Fundus coloboma
  • Interface of vitreous and retina observation
  • Retinal incarceration
  • Generalized retinal degeneration of both eyes
  • Retinal traction
  • Zonular traction retinal tuft
  • Defect of nerve fiber layer of right retina
  • Coloboma of fundus
  • Retinal pigment epithelial abnormality
  • DSM (dome shaped macula) of left eye
  • Hamartoma of retina of both eyes
  • Retinal deposits
  • Tay's spot
  • Diffuse subretinal fibrosis
  • Bilateral perifoveal capillary nonperfusion
  • Central progressive retinal atrophy
  • AMNR - acute macular neuroretinopathy
  • Macula - multifocal placoid lesions
  • Macular subretinal fibrosis
  • Methanol retinopathy
  • Purtscher retinopathy of right eye
  • Retinal depigmentation
  • Noncystic peripheral retinal tuft
  • Retinal lipid deposits
  • Right retinopathy caused by pentosan polysulfate
  • Congenital coloboma of optic disc
  • Finding of general appearance of retina
  • Subretinal fluid
  • Acute annular outer retinopathy
  • Retinal pigment epithelium atrophy
  • Congenital anomaly of left optic disc
  • Defect of nerve fibre layer of right retina
  • Congenital coloboma of bilateral optic discs
  • Fundus oculi atrophy
  • Heaping of retina
  • Myopic chorioretinal degeneration
  • Acute retinal necrosis
  • Venostasis retinopathy
  • Generalized degeneration of retina of both eyes
  • Atrophic retina
  • Bilateral defect of nerve fiber layer of retinas
  • Defect of nerve fiber layer of bilateral retinas
  • Congenital coloboma of right optic disc
  • Drug-induced retinopathy
  • Macular displacement
  • Hamartoma of retina of left eye
  • Generalized degeneration of retina of left eye
  • Hamartoma of retina of right eye
  • Multifocal progressive retinal atrophy
  • Retinal nerve fiber bundle deficiency
  • Hyperviscosity retinopathy
  • Venous stasis retinopathy
  • RPE changes
  • Retinal nerve fibre bundle defect of left eye
  • Star figure at the macula
  • Bilateral retinal deposits of eyes
  • Small isolated atrophic patches of retinal pigment epithelium
  • Myopic chorioretinal atrophy
  • Congenital anomaly of both retinas
  • Diffuse subretinal fibrosis of right eye
  • Retinal nerve fiber bundle defect of left eye
  • Vascular occlusion of retina of bilateral eyes
  • Right foveal reflex absent
  • Retinopathy as late effect of radiation
  • Hydroxychloroquine adverse reaction
  • Purtscher retinopathy of both eyes
  • Delayed rod or cone adaption
  • DSM - dome shaped macula
  • Peripheral retinal tuft
  • Cherry red macula
  • Preretinal and epiretinal finding
  • Preretinal and epiretinal observation
  • Bilateral congenital anomaly of optic disc
  • Vitreoretinal tuft
  • Retina - peripheral cystic tufts
  • Subretinal lipid deposit
  • Peripheral myopic atrophy
  • Disorder of retina of both eyes caused by pentosan polysulfate
  • Retinopathy of left eye caused by tamoxifen
  • Bilateral diffuse subretinal fibrosis
  • Necrotising herpetic retinopathy
  • Retinal fold
  • Diffuse subretinal fibrosis of bilateral eyes
  • Gross myopic retinal degeneration
  • Patchy atrophy of retinal pigment epithelium
  • General appearance of retina - finding
  • Retinal tuft
  • Nerve fibre bundle defect
  • Bilateral Purtscher retinopathy of eyes
  • Multifocal retinal degeneration
  • Dragging of retina
  • Disorder of retina caused by radiation
  • Congenital optic disc coloboma
  • Defect of nerve fiber layer of left retina
  • Zonular traction peripheral retinal tuft
  • Retinal pigment epithelial hypertrophy
  • Bilateral congenital anomaly of retinas
Frequently Asked Questions
What is the ICD-10 code for other specified retinal disorders?

The ICD-10-CM code for other specified retinal disorders is H35.89. The full clinical description is "Other specified retinal disorders". H35.89 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code H35.89 mean?

ICD-10-CM code H35.89 represents “Other specified retinal disorders”. It is classified under Chapter 7: Diseases of the Eye and Adnexa and is a billable/specific code that can be used on a claim.

Is H35.89 a billable code?

Yes, H35.89 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is H35.89 in?

H35.89 is in Chapter 7: Diseases of the Eye and Adnexa (codes H00-H59).

What SNOMED CT codes does H35.89 map to?

H35.89 maps to 133 SNOMED CT concepts: 783612007, 1234824005, 231986000, 193690006, 247144003, and 128 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for H35.89?

H35.89 is linked to 1 UMLS Concept Unique Identifier: C0348553. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does H35.89 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified retinal disorders affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of H35.89?

There is no direct ICD-11 mapping available for H35.89 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.