2024 ICD-10-CM Diagnosis Code E70.39

Approximate Synonyms

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

• Albinism-deafness syndrome of Tietz
• Dystopia canthorum
• Griscelli syndrome type 1
• Griscelli syndrome type 3
• Hypopigmentation-immunodeficiency disease
• Hypopigmentation-immunodeficiency disease
• Hypopigmentation-immunodeficiency disease
• Immunodeficiency associated with multiple organ system abnormalities
• Immunodeficiency associated with multiple organ system abnormalities
• Immunodeficiency associated with multiple organ system abnormalities
• Immunodeficiency with major anomalies
• Immunodeficiency with major anomalies
• Immunodeficiency with major anomalies
• Phylloid hypomelanosis
• Piebald trait with neurologic defects syndrome
• Piebaldism
• Profound hearing loss
• Profound sensorineural hearing loss
• Sensorineural hearing loss of bilateral ears
• Waardenburg syndrome
• Waardenburg syndrome type 3
• Ziprkowski-Margolis syndrome

Clinical Information

• Waardenburg Syndrome

  rare, autosomal dominant disease with variable penetrance and several known clinical types. characteristics may include depigmentation of the hair and skin, congenital deafness, heterochromia iridis, medial eyebrow hyperplasia, hypertrophy of the nasal root, and especially dystopia canthorum. the underlying cause may be defective development of the neural crest (neurocristopathy). waardenburg's syndrome may be closely related to piebaldism. klein-waardenburg syndrome refers to a disorder that also includes upper limb abnormalities.

• Piebaldism

  autosomal dominant, congenital disorder characterized by localized hypomelanosis of the skin and hair. the most familiar feature is a white forelock presenting in 80 to 90 percent of the patients. the underlying defect is possibly related to the differentiation and migration of melanoblasts, as well as to defective development of the neural crest (neurocristopathy). piebaldism may be closely related to waardenburg syndrome.

• Piebaldism

  a rare, autosomal dominant disorder caused usually by mutations in the kit gene. it is characterized by abnormalities in the development of melanocytes. it presents with multiple symmetrical hypopigmented or depigmented patches of skin and a midline patch of white hair.

Convert E70.39 to ICD-9-CM

• ICD-9-CM Code: 270.2 - Arom amin-acid metab NEC
  Approximate Flag - The approximate mapping means there is not an exact match between the ICD-10 and ICD-9 codes and the mapped code is not a precise representation of the original code.

Patient Education

Skin Pigmentation Disorders

Pigmentation means coloring. Skin pigmentation disorders affect the color of your skin. Your skin gets its color from a pigment called melanin. Special cells in the skin make melanin. When these cells become damaged or unhealthy, it affects melanin production. Some pigmentation disorders affect just patches of skin. Others affect your entire body.

If your body makes too much melanin, your skin gets darker. Pregnancy, Addison's disease, and sun exposure all can make your skin darker. If your body makes too little melanin, your skin gets lighter. Vitiligo is a condition that causes patches of light skin. Albinism is a genetic condition affecting a person's skin. A person with albinism may have no color, lighter than normal skin color, or patchy missing skin color. Infections, blisters and burns can also cause lighter skin.

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.