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- Be02e41f80271514afea5aaeb9de16b4f hasDbXref "Orphanet:137831" @default.
- Be02e41f80271514afea5aaeb9de16b4f type Axiom @default.
- Be02e41f80271514afea5aaeb9de16b4f annotatedProperty IAO_0000115 @default.
- Be02e41f80271514afea5aaeb9de16b4f annotatedSource MONDO_0010337 @default.
- Be02e41f80271514afea5aaeb9de16b4f annotatedTarget "X-linked intellectual deficit-cerebellar hypoplasia, also known as OPHN1 syndrome, is a rare syndromic form of cerebellar dysgenesis characterized by moderate to severe intellectual deficit and cerebellar abnormalities." @default.