Disease #01252 (PNKD-1 (dyskinesia, nonkinesigenic, paroxysmal, type 1 (PNKD-1)), OMIM:118800)

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Official abbreviation	PNKD-1
Name	dyskinesia, nonkinesigenic, paroxysmal, type 1 (PNKD-1)
OMIM ID	118800
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PNKD
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A