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MIM:615502 - MENTAL RETARDATION, AUTOSOMAL DOMINANT 21; MRD21
Echinobase Genes: ctcf
Human Disease Resource: OMIM
DOID:0070051 - autosomal dominant non-syndromic intellectual disability 21 |
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DOID:0070051 - autosomal dominant non-syndromic intellectual disability 21 |