Albinism, unspecified. E70.30 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2019 edition of ICD-10-CM E70.30 became effective on October 1, 2018.
E70.319 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2018/2019 edition of ICD-10-CM E70.319 became effective on October 1, 2018. This is the American ICD-10-CM version of E70.319 - other international versions of ICD-10 E70.319 may differ.
Ocular abnormalities may include reduced pigmentation of the iris, nystagmus, photophobia, strabismus, and decreased visual acuity. Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
Ocular albinism is a genetic condition that primarily affects the eyes. This condition reduces the coloring (pigmentation) of the iris, which is the colored part of the eye, and the retina , which is the light-sensitive tissue at the back of the eye.
8.
6 Moderate visual impairment, monocular. Visual impairment category 1 in one eye and categories 0 or 9 in other eye.
H53. 02 - Refractive amblyopia | ICD-10-CM.
When your immune system fails to respond adequately to infection, it's called an immunodeficiency, and you may be immunocompromised. People may also suffer from the opposite condition, an overactive immune system that attacks healthy cells as though they were foreign bodies, and that is called an autoimmune response.
To accurately assign the ICD-10 code D89. 9, disorder involving the immune mechanism unspecified, or D84. 9, immunodeficiency unspecified, the patient's immunocompromised state should not be attributed to a chronic condition or a prescribed medication therapy.
Blindness right eye, category 5 The 2022 edition of ICD-10-CM H54. 0X5 became effective on October 1, 2021. This is the American ICD-10-CM version of H54. 0X5 - other international versions of ICD-10 H54.
ICD-10 code H54. 0 for Blindness, both eyes is a medical classification as listed by WHO under the range - Diseases of the eye and adnexa .
Visual impairment is the term used to describe a loss of sight that cannot be corrected using glasses or contact lenses.
Refractive amblyopia, unspecified eye H53. 029 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2022 edition of ICD-10-CM H53. 029 became effective on October 1, 2021.
0 - Hypermetropia. H52. 0 - Hypermetropia is a topic covered in the ICD-10-CM.
Lazy eye (amblyopia) is reduced vision in one eye caused by abnormal visual development early in life. The weaker — or lazy — eye often wanders inward or outward. Amblyopia generally develops from birth up to age 7 years. It is the leading cause of decreased vision among children. Rarely, lazy eye affects both eyes.
Non-specific codes like E70.31 require more digits to indicate the appropriate level of specificity. Consider using any of the following ICD-10 codes with a higher level of specificity when coding for ocular albinism:
ALBINISM OCULAR-. albinism affecting the eye in which pigment of the hair and skin is normal or only slightly diluted. the classic type is x linked nettleship falls but an autosomal recessive form also exists. ocular abnormalities may include reduced pigmentation of the iris nystagmus photophobia strabismus and decreased visual acuity.
Some eye problems are minor and don't last long. But some can lead to a permanent loss of vision.
Piebaldism is a rare autosomal dominant disorder of melanocyte development.:867 Common characteristics include a congenital white forelock, scattered normal pigmented and hypopigmented macules and a triangular shaped depigmented patch on the forehead.
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E70.31. Click on any term below to browse the alphabetical index.
People with albinism may have vision problems and white or yellow hair; reddish, violet, blue or brown eyes; and pale skin. General term for a number of inherited defects of amino acid metabolism in which there is a deficiency or absence of pigment in the eyes, skin, or hair.
A congenital disorder characterized by partial or complete absence of melanin pigment in the eyes, hair and skin. A group of genetic conditions marked by little or none of the pigment melanin in the skin, hair, and/or eyes. People with albinism may have vision problems and white or yellow hair; reddish, violet, blue or brown eyes; and pale skin.