Landau-Kleffner syndrome

Summary

DOID:2538 - Landau-Kleffner syndrome

Disease Ontology Definition:A childhood electroclinical syndrome that is characterized by the loss of language comprehension (auditory verbal agnosia) and verbal expression (aphasia) in association with severely abnormal electroencephalographic (EEG) findings during sleep and clinical seizures in most patients.

Synonyms: acquired epileptic aphasia

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: grin2a

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0009509 - Landau-Kleffner syndrome

MONDO:0009509 - Landau-Kleffner syndrome

MIM:

MIM:245570 - EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; FESD

MIM:245570 - EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; FESD

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): childhood electroclinical syndrome (is_a)