# Ogden syndrome

> X-linked disease resulting from a deficiency in N-terminal acetyltransferase, extreme abrupt behavior, anger issues, characterized by postnatal growth failure with severe delays and dysmorphic features in boys

**Wikidata**: [Q17144188](https://www.wikidata.org/wiki/Q17144188)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Ogden_syndrome)  
**Source**: https://4ort.xyz/entity/ogden-syndrome


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000102030/MONDO_0010457)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000102030/Orphanet_276432)
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)