Ogden syndrome
Information
- Disease name
- Ogden syndrome
- Disease ID
- DOID:0050781
- Description
- "A syndrome characterized by postnatal growth failure, severely delayed psychomotor development, variable dysmorphic features, and hypotonia and has_material_basis_in X-linked recessive or X-linked dominant mutation in the NAA10 gene on chromosome Xq28." [url:https\://en.wikipedia.org/wiki/Ogden_syndrome, url:https\://www.ncbi.nlm.nih.gov/pubmed/21700266]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:225
- Cross Reference ID (Disease Ontology)
- MIM:300855
- Cross Reference ID (Disease Ontology)
- ORDO:276432
- Exact Synonym (Disease Ontology)
- N-alpha-acetyltransferase
- Exact Synonym (Disease Ontology)
- N-terminal acetyltransferase deficiency
- Exact Synonym (Disease Ontology)
- OGDNS
- Exact Synonym (Disease Ontology)
- X-linked Malformation and Infantile Lethality Syndrome
- OrphaNumber from OrphaNet (Orphanet)
- 276432