Genetics

CDKN1C gene

AKT3 gene

X-linked agammaglobulinemia

Ataxia with oculomotor apraxia

RSPO2 gene

Type A insulin resistance syndrome

Cleidocranial dysplasia

Epidermal nevus

Glycogen storage disease type I

RUNX1T1 gene

PEX7 gene

MT-ND4L gene