Disease #00319 (PCH-6 (hypoplasia, pontocerebellar, type 6 (PCH-6)), OMIM:611523)

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	Curator: Johan T. den Dunnen

Official abbreviation	PCH-6
Name	hypoplasia, pontocerebellar, type 6 (PCH-6)
OMIM ID	611523
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RARS2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-02-02 21:24:34 +01:00 (CET)
Date last edited	N/A