Klippel-Feil syndrome 3, autosomal dominant

MONDO:0013375

Any isolated Klippel-Feil syndrome in which the cause of the disease is a mutation in the GDF3 gene.

Also known as: GDF3 isolated Klippel-Feil syndrome, Klippel-Feil syndrome 3, autosomal dominant, isolated Klippel-Feil syndrome caused by mutation in GDF3, KFS3, Klippel-FEIL syndrome 3, autosomal dominant

0 clinical trials for this condition and its sub-types, 0 tagged with Klippel-Feil syndrome 3, autosomal dominant itself.

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Including sub-types (0) Tagged with Klippel-Feil syndrome 3, autosomal dominant (0)

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