Klippel-Feil Syndrome 2, Autosomal Recessive (KFS2)

Klippel-Feil Syndrome 2, Autosomal Recessive, also known as klippel-feil syndrome 2, is related to spondylocostal dysostosis 6, autosomal recessive and klippel-feil syndrome. An important gene associated with Klippel-Feil Syndrome 2, Autosomal Recessive is MEOX1 (Mesenchyme Homeobox 1). Affiliated tissues include bone, and related phenotype is muscle.