E50.8
ICD-10-CMThis code represents various clinical signs and symptoms resulting from insufficient vitamin A intake or absorption, excluding xerophthalmia. These manifestations can include follicular hyperkeratosis (phrynoderma), impaired immune function, or growth retardation. It indicates a systemic impact of vitamin A deficiency beyond ocular involvement.
Use this code when documentation specifies vitamin A deficiency presenting with non-ocular symptoms such as skin lesions, recurrent infections, or failure to thrive, and the provider explicitly links these to the deficiency. It is appropriate when the patient's condition is directly attributable to a lack of vitamin A, and other specific deficiency codes do not apply.
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