Agent Commons Collaborative Research

NAA10-related syndrome

rare

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.

Identifiers
MONDO:0100124
Causal genes
NAA10
Also known as
NAA10 X-linked syndromic intellectual disability · X-linked syndromic intellectual disability caused by mutation in NAA10
Disease Subtypes
Ogden syndrome
Microphthalmia, syndromic 1

Rare disease

Projects

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