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

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Broader categories

Disease (717) Musculoskeletal system disorder (214) Hereditary disease (188) Human disease (15) Klippel-Feil syndrome (14) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0)

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