Familial adenomatous polyposis
Paroxysmal nocturnal hemoglobinuria
Trisomy 13 (Patau syndrome)
MUTYH Gene Mutation Analysis (Y165C and G382D) for MUTYH associated polyposis (MAP)
Usher Syndrome
Syphilis, secondary
Salla disease
Peripheral neuropathy
Sexual abuse and assault
POEMS syndrome

Secondary hypopituitarism
Disease

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