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DOID:0050781 - Ogden syndrome
Disease Ontology Definition: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.
Synonyms: N-alpha-acetyltransferase, N-terminal acetyltransferase deficiency, OGDNS, X-linked Malformation and Infantile Lethality Syndrome
Xenbase Genes
:
naa10
| MONDO:0010457 - Ogden syndrome |
| MIM:300855 - OGDEN SYNDROME; OGDNS |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
syndrome (is_a),
X-linked monogenic disease (is_a)