Disease #05835 (EPRPDC (epilepsy, rolandic, with proxysmal exercise-induce dystonia and writer's cramp (EPRPDC)), OMIM:608105)

Official abbreviation EPRPDC
Name epilepsy, rolandic, with proxysmal exercise-induce dystonia and writer's cramp (EPRPDC)
OMIM ID 608105
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene TBC1D24
Associated tissues -
Disease features -
Remarks -
Date created 2020-09-18 16:18:07 +02:00 (CEST)
Date last edited N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.