Disease #06972 (PCH17 (hypoplasia, pontocerebellar, type 17), OMIM:619909)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	PCH17
Name	hypoplasia, pontocerebellar, type 17
OMIM ID	619909
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PRDM13
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-10-17 11:06:47 +02:00 (CEST)
Date last edited	N/A

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