Genetics

Kearns-Sayre syndrome

WNT5A gene

Stüve-Wiedemann syndrome

Melorheostosis

ALAS2 gene

Asparagine synthetase deficiency

Multicentric osteolysis nodulosis and arthropathy

Schimke immuno-osseous dysplasia

Core binding factor acute myeloid leukemia

SOX2 anophthalmia syndrome

RPS14 gene

Adermatoglyphia