Meier-Gorlin syndrome 1
MONDO:0009143Any Meier-Gorlin syndrome in which the cause of the disease is a mutation in the ORC1 gene.
Also known as: Meier-Gorlin syndrome 1, Meier-Gorlin syndrome caused by mutation in ORC1, Meier-Gorlin syndrome type 1, ORC1 Meier-Gorlin syndrome, Ear, patella, short stature syndrome, MGORS1, Meier-GORLIN syndrome 1, Meier-Gorlin syndrome
0 clinical trials for this condition and its sub-types.
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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
(1)
Autosomal genetic disease
(0)
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