Meier-Gorlin syndrome 7
MONDO:0014894Any Meier-Gorlin syndrome in which the cause of the disease is a mutation in the CDC45 gene.
Also known as: CDC45 Meier-Gorlin syndrome, MGORS7, Meier-Gorlin syndrome 7, Meier-Gorlin syndrome 7; MGORS7, Meier-Gorlin syndrome caused by mutation in CDC45, Meier-Gorlin syndrome type 7
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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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Autosomal recessive disease
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Disease of genetic or genomic mechanism
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Meier-Gorlin syndrome
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Multiple congenital anomalies/dysmorphic syndrome
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Autosomal genetic disease
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