- OMIM ID
-
608027
- OMIM term:
- PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3
- Alternative terms:
-
CEREBELLAR ATROPHY WITH PROGRESSIVE MICROCEPHALY; CLAM
PCH WITH OPTIC ATROPHY
- (∗) Location:
- 7q11-q21
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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