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Up to: X-linked syndromic intellectual disability
NAA10-related syndrome
Ab X-linked syndromic intellectual disability in which the cause of the disease is a mutation in the NAA10 gene. Patients with variants in the NAA10 gene demonstrate symptoms such as developmental delay, intellectual disability, autism spectrum disorder, hypotonia, facial dysmorphism, cardiac anomalies, and/or skeletal anomalies.
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Ogden syndrome 0 trials
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Microphthalmia, syndromic 1 0 trials