Human genes for Klippel-Feil syndrome 2
Klippel-Feil syndrome 2 [DOID:0080590]
A Klippel-Feil syndrome that has_material_basis_in homozygous mutation in the MEOX1 gene on chromosome 17q21.
Synonyms: Klippel-Feil syndrome 2, DOID:0080590, KlippelFeil syndrome 2