• Glanzmann thrombasthenia (hereditary familial thrombocytopenia)
  • Trypanosomiasis meningitis
  • Cologaurd®, Cologuard Plus, Stool DNA-Based Colorectal Cancer Screening Test
  • Malignant Neoplasms, Bone and articular cartilage (Osteosarcoma)
  • Secondary hypopituitarism
  • Familial adenomatous polyposis
  • Paroxysmal nocturnal hemoglobinuria
  • Trisomy 13 (Patau syndrome)
  • MUTYH Gene Mutation Analysis (Y165C and G382D) for MUTYH associated polyposis (MAP)
  • Usher Syndrome
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Cowden Syndrome
Disease

Additional ICD10
Access to Cowden Syndrome is restricted.
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