Disease #02852 (PNKD3;GEPD (dyskinesia, nonkinesigenic, paroxysmal, type 3, with/without generalized epilepsy (PNKD-3, generalized epilepsy and paroxysmal dyskinesia(GEPD))), OMIM:609446)

Official abbreviation PNKD3;GEPD
Name dyskinesia, nonkinesigenic, paroxysmal, type 3, with/without generalized epilepsy (PNKD-3, generalized epilepsy and paroxysmal dyskinesia(GEPD))
OMIM ID 609446
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene KCNMA1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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