Klippel-Feil syndrome 2, autosomal recessive

Any isolated Klippel-Feil syndrome in which the cause of the disease is a mutation in the MEOX1 gene.

Also known as: Klippel-Feil syndrome 2, autosomal recessive, MEOX1 isolated Klippel-Feil syndrome, isolated Klippel-Feil syndrome caused by mutation in MEOX1, KFS2, Kfs, autosomal recessive, Klippel-FEIL syndrome 2, autosomal recessive, cervical vertebral fusion, autosomal recessive

32 clinical trials for this condition and its sub-types.