Molybdenum deficiency

This code signifies a nutritional deficiency specifically related to molybdenum, an essential trace element. Molybdenum acts as a cofactor for several enzymes crucial for metabolic processes, including sulfur metabolism and detoxification. A deficiency can lead to various non-specific symptoms affecting neurological function, growth, and overall metabolic health.

Apply this code when documentation clearly indicates a diagnosis of molybdenum deficiency, often supported by laboratory findings showing low molybdenum levels. This may be seen in patients with genetic metabolic disorders affecting molybdenum metabolism, or in rare cases of severe malnutrition or prolonged parenteral nutrition without adequate supplementation.

• Ensure documentation specifies "molybdenum" deficiency, not a general mineral deficiency.
• Consider sequencing this code after any underlying genetic or metabolic disorder contributing to the deficiency.
• Look for supporting lab results (e.g., plasma or urine molybdenum levels) or clinical signs consistent with enzymatic dysfunction.