Disease #05964 (DEE59 (encephalopathy, developmental and epileptic, type 59), OMIM:617904)

Official abbreviation DEE59
Name encephalopathy, developmental and epileptic, type 59
OMIM ID 617904
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene GABBR2
Associated tissues -
Disease features -
Remarks -
Date created 2021-08-11 11:46:07 +02:00 (CEST)
Date last edited 2023-10-23 16:03:07 +02:00 (CEST)


Individuals

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00435325 256529 - - F no Germany - - - - - DEE59 Global developmental delay, Dysmetria, Dyskinesia, Ataxia GABBR2 GABBR2 1 1 Andreas Laner
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