All diseases

OMIM ID
277470
OMIM term:
PONTOCEREBELLAR HYPOPLASIA, TYPE 2A; PCH2A
Alternative terms:
PCH2
PONTOCEREBELLAR HYPOPLASIA WITH PROGRESSIVE CEREBRAL ATROPHY
VOLENDAM NEURODEGENERATIVE DISEASE
(∗) Location:
17q25.1  
(†) Associated OMIM genes:
TSEN54  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/09nji17u