Any isolated Klippel-Feil syndrome in which the cause of the disease is a mutation in the MEOX1 gene.
Comprehensive, easy-to-understand information about this condition
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Gene data from MyGene.info • Click to view on NCBI Gene
Klippel-Feil syndrome 1, autosomal dominant
MONDO:0007306
Wildervanck syndrome
MONDO:0010759
Klippel-Feil syndrome 3, autosomal dominant
MONDO:0013375
Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome
MONDO:0014689
Calabro syndrome
MONDO:0022055