Genetics

Hand-foot-genital syndrome

UV-sensitive syndrome

UNC80 deficiency

21-hydroxylase deficiency

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy

Coffin-Lowry syndrome

Kaufman oculocerebrofacial syndrome

Choroideremia

MSX2 gene

IL2RG gene

POGZ gene

Spastic paraplegia type 31