2024 ICD-10-CM Diagnosis Code H35.00

Unspecified background retinopathy

ICD-10-CM Code:
H35.00
ICD-10 Code for:
Unspecified background retinopathy
Is Billable?
Yes - Valid for Submission
Chronic Condition Indicator: [1]
Chronic
Code Navigator:

Code Classification

  • Diseases of the eye and adnexa
    (H00–H59)
    • Disorders of choroid and retina
      (H30-H36)
      • Other retinal disorders
        (H35)

H35.00 is a billable diagnosis code used to specify a medical diagnosis of unspecified background retinopathy. The code is valid during the current fiscal year for the submission of HIPAA-covered transactions from October 01, 2023 through September 30, 2024.

Unspecified diagnosis codes like H35.00 are acceptable when clinical information is unknown or not available about a particular condition. Although a more specific code is preferable, unspecified codes should be used when such codes most accurately reflect what is known about a patient's condition. Specific diagnosis codes should not be used if not supported by the patient's medical record.

Approximate Synonyms

The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:

  • Acute zonal occult outer retinopathy
  • Adverse reaction to Cinchona alkaloid
  • Aminoquinoline antimalarial adverse reaction
  • Aminoquinoline antimalarial adverse reaction
  • Autosomal recessive chorioretinopathy and microcephaly syndrome
  • Background retinopathy due to impaired glucose regulation
  • Bilateral retinopathy
  • Bilateral retinopathy of eyes caused by hydroxychloroquine
  • Chelating agent adverse reaction
  • Chloroquine adverse reaction
  • Chloroquine retinopathy
  • Desferrioxamine adverse reaction
  • Desferrioxamine retinopathy
  • Disorder of blood vessel of retina of left eye
  • Disorder of blood vessel of retina of right eye
  • Estrogen antagonist adverse reaction
  • Familial aplasia of the vermis
  • Hereditary vitreoretinopathy
  • Hydrochloroquine retinopathy
  • Hydroxychloroquine adverse reaction
  • Joubert syndrome
  • Joubert syndrome with ocular defect
  • Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome
  • Paraneoplastic retinopathy
  • Quinine adverse reaction
  • Quinine retinopathy
  • Renal retinopathy
  • Retinal vascular disorder
  • Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
  • Retinopathy caused by canthaxanthin
  • Retinopathy caused by trifluoperazine
  • Retinopathy due to atherosclerosis
  • Retinopathy of left eye caused by hydroxychloroquine
  • Retinopathy of right eye caused by hydroxychloroquine
  • Small vessel cerebrovascular disease
  • Tamoxifen adverse reaction
  • Tamoxifen retinopathy
  • Thioridazine adverse reaction
  • Thioridazine retinopathy
  • Trifluoperazine adverse reaction
  • Vascular retinopathy of bilateral eyes

Clinical Classification

Clinical Information

  • Joubert Syndrome

    a rare genetic syndrome characterized by the hypoplasia or absence of the cerebellar vermis. signs and symptoms include rapid breathing (hyperpnea), sleep apnea, abnormal eye movements, mental retardation, and ataxia.
  • Joubert Syndrome 17|JBTS17

    an autosomal recessive subtype of joubert syndrome caused by mutation(s) in the cplane1 gene, encoding ciliogenesis and planar polarity effector 1.
  • Joubert Syndrome 3|JBTS3

    an autosomal recessive subtype of joubert syndrome caused by mutation(s) in the ahi1 gene, encoding jouberin.
  • Joubert Syndrome 4

    a rare genetic syndrome caused by mutations in the nphp1 gene. it is characterized by the hypoplasia or absence of the cerebellar vermis. signs and symptoms include rapid breathing (hyperpnea), sleep apnea, abnormal eye movements, mental retardation, and ataxia.
  • Joubert Syndrome 7|JBTS7

    an autosomal recessive sub-type of joubert syndrome caused by mutation(s) in the rpgrip1l gene, encoding a protein thought to function in programmed cell death. it is characterized by cerebellar and oculomotor apraxia, hypotonia and psychomotor delay, neonatal respiratory abnormalities, renal abnormalities, and retinal dystrophy.
  • Joubert Syndrome 9|JBTS9

    an autosomal recessive subtype of joubert syndrome caused by mutation(s) in the cc2d2a gene, encoding coiled-coil and c2 domain-containing protein 2a.

Index to Diseases and Injuries References

The following annotation back-references for this diagnosis code are found in the injuries and diseases index. The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10-CM code(s).

Convert H35.00 to ICD-9-CM

  • ICD-9-CM Code: 362.10 - Backgrnd retinopathy NOS

Patient Education


Retinal Disorders

The retina is a layer of tissue in the back of your eye that senses light and sends images to your brain. In the center of this nerve tissue is the macula. It provides the sharp, central vision needed for reading, driving and seeing fine detail.

Retinal disorders affect this vital tissue. They can affect your vision, and some can be serious enough to cause blindness. Examples are:

  • Macular degeneration - a disease that destroys your sharp, central vision
  • Diabetic eye disease
  • Retinal detachment - a medical emergency, when the retina is pulled away from the back of the eye
  • Retinoblastoma - cancer of the retina. It is most common in young children.
  • Macular pucker - scar tissue on the macula
  • Macular hole - a small break in the macula that usually happens to people over 60
  • Floaters - cobwebs or specks in your field of vision

NIH: National Eye Institute


[Learn More in MedlinePlus]

Code History

  • FY 2024 - No Change, effective from 10/1/2023 through 9/30/2024
  • FY 2023 - No Change, effective from 10/1/2022 through 9/30/2023
  • FY 2022 - No Change, effective from 10/1/2021 through 9/30/2022
  • FY 2021 - No Change, effective from 10/1/2020 through 9/30/2021
  • FY 2020 - No Change, effective from 10/1/2019 through 9/30/2020
  • FY 2019 - No Change, effective from 10/1/2018 through 9/30/2019
  • FY 2018 - No Change, effective from 10/1/2017 through 9/30/2018
  • FY 2017 - No Change, effective from 10/1/2016 through 9/30/2017
  • FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016. This was the first year ICD-10-CM was implemented into the HIPAA code set.

Footnotes

[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:

  • The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
  • The condition places limitations on self-care, independent living, and social interactions.