Van der Woude syndrome 2
MONDO:0011712Any van der Woude syndrome in which the cause of the disease is a mutation in the GRHL3 gene.
Also known as: GRHL3 van der Woude syndrome, Van Der Woude syndrome type 2, van der Woude syndrome 2, van der Woude syndrome caused by mutation in GRHL3, VAN DER Woude syndrome 2, VWS2
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Disease
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Hereditary disease
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Syndromic disease
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Human disease
(14)
Developmental defect during embryogenesis
(8)
Van der Woude syndrome
(8)
Disease of genetic or genomic mechanism
(2)
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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