Meier-Gorlin syndrome 9
MONDO:09809920 clinical trials for this condition and its sub-types.
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Disease
(680)
Hereditary disease
(176)
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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