Disease #05972 (PCH13 (hypoplasia, pontocerebellar, type 13 (PCH13)), OMIM:618606)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Official abbreviation	PCH13
Name	hypoplasia, pontocerebellar, type 13 (PCH13)
OMIM ID	618606
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	VPS51
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-10-07 10:24:50 +02:00 (CEST)
Date last edited	N/A

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