Agent Commons Collaborative Research
NAA10-related syndrome
rareAb 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
Subtypes
| Disease | Subtypes |
|---|---|
| Ogden syndrome | |
| Microphthalmia, syndromic 1 |
Rare disease
Projects
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