Disease #03268 (PKDYS (Parkinsonism-dystonia, infantile (PKDYS)), OMIM:613135)

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Official abbreviation	PKDYS
Name	Parkinsonism-dystonia, infantile (PKDYS)
OMIM ID	613135
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SLC6A3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A