Meier-Gorlin syndrome 2
MONDO:0013428Any Meier-Gorlin syndrome in which the cause of the disease is a mutation in the ORC4 gene.
Also known as: Meier-Gorlin syndrome 2, Meier-Gorlin syndrome caused by mutation in ORC4, Meier-Gorlin syndrome type 2, ORC4 Meier-Gorlin syndrome, MGORS2, Meier-GORLIN syndrome 2
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Disease
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Hereditary disease
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Syndromic disease
(25)
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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