|
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 :
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)