icd-10 code for x-lined ocular albinism

What is the ICD 10 code for ocular albinism?

X-linked ocular albinism. 2016 2017 2018 2019 Billable/Specific Code. E70.310 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 E70.310 became effective on October 1, 2018.

What is the medical term for albinism?

Albinism, unspecified. 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. Inherited disease where in which there is a deficiency or absence of pigment in the eyes, skin, or hair.

What is the ICD 10 code for uveitis?

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.

What is an ocular abnormality?

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.

What is ocular albinism?

Ocular albinism is a genetic disorder characterized by vision abnormalities in affected males. Vision deficits are present at birth and do not become more severe over time. Affected individuals have normal skin and hair pigmentation.

What is the ICD-10 code for immunodeficiency with partial albinism?

8.

What is the ICD-10-CM code for congenital nystagmus?

ICD-10 code H55. 01 for Congenital nystagmus is a medical classification as listed by WHO under the range - Diseases of the eye and adnexa .

What is the ICD-10 code for alcohol abuse?

ICD-10 code F10. 2 for Alcohol dependence is a medical classification as listed by WHO under the range - Mental, Behavioral and Neurodevelopmental disorders .

What is diagnosis code d849?

9: Immunodeficiency, unspecified.

Is Immunodeficiency the same as immunocompromised?

People with immunodeficiency or autoimmune disease are considered immunocompromised, but other factors can also cause someone to be immunocompromised, such as cancer, cancer treatments, metabolic disorders or advanced age, according to The University of Texas MD Anderson Cancer Center.

What is congenital nystagmus?

Abstract. Infantile nystagmus (IN), previously known as congenital nystagmus, is an involuntary to-and-fro movement of the eyes that persists throughout life. IN is one of three types of early-onset nystagmus that begin in infancy, alongside fusion maldevelopment nystagmus syndrome and spasmus nutans syndrome.

What nystagmus means?

Nystagmus is an involuntary rhythmic side-to-side, up and down or circular motion of the eyes that occurs with a variety of conditions.

What is horizontal nystagmus?

Nystagmus is a condition where the eyes move rapidly and uncontrollably. They can move: side to side (horizontal nystagmus) up and down (vertical nystagmus) in a circle (rotary nystagmus)

What diagnosis is F10 10?

Based upon the DSM-5 criteria, the patient appears to have a diagnosis of Alcohol Use Disorder (Mild) (ICD-10 code F10. 10).

What is DX code f10129?

129.

What does F10 20 mean?

F10. 20 - Alcohol dependence, uncomplicated | ICD-10-CM.

The ICD code E703 is used to code Piebaldism

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.

ICD-10-CM Alphabetical Index References for 'E70.310 - X-linked ocular albinism'

The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E70.310. Click on any term below to browse the alphabetical index.

Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)

This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code E70.310 and a single ICD9 code, 270.2 is an approximate match for comparison and conversion purposes.

The ICD code E703 is used to code Piebaldism

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.

ICD-10-CM Alphabetical Index References for 'E70.31 - Ocular albinism'

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.

What does albinism look like?

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.

What is the name of the condition where you have no pigment in your eyes?

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.