has material basis in germline mutation in MEOX1 Klippel-Feil syndrome Klippel-Feil syndrome 2, autosomal recessive https://github.com/monarch-initiative/mondo/issues/4948 https://www.malacards.org/card/klippel_feil_syndrome_2 https://www.malacards.org/card/klippel_feil_syndrome_2_autosomal_recessive Klippel-FEIL syndrome 2, autosomal recessive Klippel-Feil syndrome 2, autosomal recessive MONDO:0008958 MEDGEN:395201 Kfs, autosomal recessive MEOX1 isolated Klippel-Feil syndrome DOID:0080590 isolated Klippel-Feil syndrome caused by mutation in MEOX1 MESH:C536888 cervical vertebral fusion, autosomal recessive OMIM:214300 Any isolated Klippel-Feil syndrome in which the cause of the disease is a mutation in the MEOX1 gene. GARD:0015151 UMLS:C1859209 KFS2