Genetics

Familial glucocorticoid deficiency

Crohn’s disease

MAOA gene

X-linked adrenoleukodystrophy

Bipolar disorder

Amish lethal microcephaly

PDGFRB-associated chronic eosinophilic leukemia

Nonsyndromic paraganglioma

VLDLR-associated cerebellar hypoplasia

AMHR2 gene

OPN1MW gene

Isolated ectopia lentis