In simple words: This code refers to problems with how the body processes zinc, an essential mineral. It includes a rare inherited condition called acrodermatitis enteropathica.

This code encompasses disorders related to zinc metabolism, including acrodermatitis enteropathica, a rare hereditary form of zinc deficiency.These disorders can manifest as a range of symptoms due to impaired zinc absorption or utilization.

Example 1: A 6-month-old infant, recently weaned from breast milk, develops a rash around the mouth and anus, along with diarrhea and hair loss. Diagnosis of acrodermatitis enteropathica is confirmed with low serum zinc levels. Treatment with zinc supplements is initiated., A patient with Crohn's disease experiences chronic diarrhea and malabsorption, leading to zinc deficiency. Supplementation is prescribed to correct the deficiency and prevent further complications., A premature infant on parenteral nutrition develops symptoms of zinc deficiency. The nutritional solution is reviewed and supplemented with zinc to meet the infant's increased metabolic demands.

Documentation should include details of the patient's clinical presentation, relevant medical history (e.g., dietary habits, malabsorption syndromes, genetic conditions), laboratory results (serum zinc levels, other micronutrient levels), and response to treatment. For acrodermatitis enteropathica, genetic testing can confirm the diagnosis.

** The information provided is current as of November 30, 2024.For the most up-to-date information and coding guidelines, always refer to the latest ICD-10-CM coding manual and reputable medical billing resources.