Disease #05332 (PCH11 (hypoplasia, pontocerebellar, non-degenerative, type 11 (PCH-11)), OMIM:617695)

Global Variome shared LOVD

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Official abbreviation	PCH11
Name	hypoplasia, pontocerebellar, non-degenerative, type 11 (PCH-11)
OMIM ID	617695
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TBC1D23
Associated tissues	-
Disease features	-
Remarks	-
Date created	2017-10-02 22:12:22 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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