Meier-Gorlin syndrome 3
MONDO:0013430Any Meier-Gorlin syndrome in which the cause of the disease is a mutation in the ORC6 gene.
Also known as: Meier-Gorlin syndrome 3, Meier-Gorlin syndrome caused by mutation in ORC6, Meier-Gorlin syndrome type 3, ORC6 Meier-Gorlin syndrome, MGORS3, Meier-GORLIN syndrome 3
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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)
Autosomal recessive disease
(4)
Disease of genetic or genomic mechanism
(2)
Meier-Gorlin syndrome
(1)
Multiple congenital anomalies/dysmorphic syndrome
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Autosomal genetic disease
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