Disease #06011 (PCH2F (hypoplasia, pontocerebellar, type 2F), OMIM:617026)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	PCH2F
Name	hypoplasia, pontocerebellar, type 2F
OMIM ID	617026
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TSEN15
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	2022-10-17 11:08:15 +02:00 (CEST)

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