Albinism
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.
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.
E70.30 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
The 2023 edition of ICD-10-CM E70.30 became effective on October 1, 2022.
This is the American ICD-10-CM version of E70.30 – other international versions of ICD-10 E70.30 may differ.