Van der Woude syndrome 1
MONDO:0007333Any van der Woude syndrome in which the cause of the disease is a mutation in the IRF6 gene.
Also known as: IRF6 van der Woude syndrome, Van Der Woude syndrome type 1, van der Woude syndrome 1, van der Woude syndrome caused by mutation in IRF6, VAN DER Woude syndrome 1, VWS1, Vdws, cleft lip and/or palate with mucous cysts of Lower lip
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Disease
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Hereditary disease
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Syndromic disease
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Human disease
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Developmental defect during embryogenesis
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Van der Woude syndrome
(8)
Disease of genetic or genomic mechanism
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Multiple congenital anomalies/dysmorphic syndrome
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Disease by body system or component
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Disease by developmental or physiological process
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