Disease #00832 (RESDX (epilepsy, Rolandic, mental retardation, and speech dyspraxia (RESDX)), OMIM:300643)

Official abbreviation RESDX
Name epilepsy, Rolandic, mental retardation, and speech dyspraxia (RESDX)
OMIM ID 300643
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene SRPX2
Associated tissues -
Disease features -
Remarks -

  Powered by LOVD v.3.0 Build 27
LOVD software ©2004-2022 Leiden University Medical Center 		There are currently no updates.