|
DOID:0080227 - autosomal dominant intellectual developmental disorder 55
Disease Ontology Definition:An autosomal dominant intellectual developmental disorder that is characterized by onset of myoclonic seizures in the first years of life, global developmental delay, intellectual disability, speech delay and ataxic gait that has_material_basis_in heterozygous mutation in the NUS1 gene on chromosome 6q22.
Synonyms: autosomal dominant intellectual developmental disorder-55 with seizures, autosomal dominant mental retardation 55,
Echinobase Genes
:
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee