All diseases

OMIM ID
225753
OMIM term:
PONTOCEREBELLAR HYPOPLASIA, TYPE 4; PCH4
Alternative terms:

(∗) Location:
17q25.1  
(†) Associated OMIM genes:
TSEN54  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/qf2ltzwr