Genetics

F5 gene

Nonsyndromic holoprosencephaly

Familial erythrocytosis

KL gene

Attention-deficithyperactivity disorder

CLN3 disease

LAMA2-related muscular dystrophy

Primary macronodular adrenal hyperplasia

Carpal tunnel syndrome

AGA gene

Bohring-Opitz syndrome

Gastrointestinal stromal tumor