Split hand-foot malformation 6
MONDO:0009157Any split hand-foot malformation in which the cause of the disease is a mutation in the WNT10B gene.
Also known as: SHFM6, WNT10B split hand-foot malformation, split hand-foot malformation caused by mutation in WNT10B, split hand-foot malformation type 6, split-hand/foot malformation type 6, ectrodactyly, autosomal recessive, split-hand/foot malformation 6
35 clinical trials for this condition and its sub-types.
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Disease
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Musculoskeletal system disorder
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Hereditary disease
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Bone disorder
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Human disease
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Skeletal system disorder
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Bone development disease
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Disease of genetic or genomic mechanism
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Disease by body system or component
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Disease by developmental or physiological process
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