Klippel-Feil syndrome 2, autosomal recessive

MONDO:0008958

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

0 clinical trials for this condition and its sub-types, 0 tagged with Klippel-Feil syndrome 2, autosomal recessive itself.

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Including sub-types (0) Tagged with Klippel-Feil syndrome 2, autosomal recessive (0)

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