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MIM:616449 - BASEL-VANAGAITE-SMIRIN-YOSEF SYNDROME; BVSYS
Xenbase Genes: med25
Human Disease Resource: MIM
| MONDO:0014643 - congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome |
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| MONDO:0014643 - congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome |