Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Echinobase
Summary Literature (0)
MIM:613811 - PONTOCEREBELLAR HYPOPLASIA, TYPE 2D; PCH2D

Echinobase Genes: sepsecs

Human Disease Resource: OMIM


Disease Ontology (DO):
DOID:0060270 - pontocerebellar hypoplasia type 2D