Genetics

Müllerian aplasia and hyperandrogenism

Beckwith-Wiedemann syndrome

NPC2 gene

CTSA gene

Tyrosine hydroxylase deficiency

SPTLC1 gene

CDH23 gene

LEP gene

Lafora progressive myoclonus epilepsy

Sickle cell disease

Ménière disease

Monoamine oxidase A deficiency