n-terminal acetyltransferase deficiency Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An X-linked disease resulting from a deficiency in N-terminal acetyltransferase, characterized by postnatal growth failure with severe delays and dysmorphic features in boys. (Human Disease Ontology, DOID_0050781)
External Link http://www.omim.org/entry/300855
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1 genes associated with the n-terminal acetyltransferase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit