- OMIM ID
-
118420
- OMIM term:
- CHIARI MALFORMATION TYPE I
- Alternative terms:
-
CM1 CHIARI MALFORMATION TYPE I WITH SYRINGOMYELIA, INCLUDED
CM1 WITH SYRINGOMYELIA, INCLUDED
- (∗) Location:
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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