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What is CPT Code 96372

Hereditary folate malabsorption Hereditary folate malabsorption is caused by mutations in the SLC46A1 gene coding for the folate transporter PCFT and typically affects gastrointestinal folate absorption and folate transport into the brain (183)

If a device makes medical claims for treating erectile dysfunction, it would need to comply with the UK Medical Devices Regulations 2002 and bear UKCA (or CE) marking, demonstrating conformity with safety and performance requirements

Confirm Zofran tolerance or no allergy