Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Echinobase
Summary Literature (0)
DOID:0050781 - Ogden syndrome

Disease Ontology Definition: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.

Synonyms: N-alpha-acetyltransferase, N-terminal acetyltransferase deficiency, OGDNS, X-linked Malformation and Infantile Lethality Syndrome,

Echinobase Genes :


OMIM:
MIM:300855 - ogden syndrome; ogdns

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): X-linked disease (is_a)