Microcephaly 27, primary, autosomal dominant
MONDO:0030929Also known as: MCPH27, microcephaly 27, primary, autosomal dominant
0 clinical trials for this condition and its sub-types.
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Disease
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Nervous system disorder
(231)
Hereditary disease
(176)
Neurodevelopmental disorder
(147)
Human disease
(14)
Developmental defect during embryogenesis
(8)
Hereditary neurological disease
(6)
Microcephaly
(4)
Disease of genetic or genomic mechanism
(2)
Congenital nervous system disorder
(1)
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