Meier-Gorlin syndrome 4
MONDO:0013431Any Meier-Gorlin syndrome in which the cause of the disease is a mutation in the CDT1 gene.
Also known as: CDT1 Meier-Gorlin syndrome, Meier-Gorlin syndrome 4, Meier-Gorlin syndrome caused by mutation in CDT1, Meier-Gorlin syndrome type 4, MGORS4, Meier-GORLIN syndrome 4
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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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