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MIM:614563 - MENTAL RETARDATION, AUTOSOMAL DOMINANT 13; MRD13
Echinobase Genes: dync1h1
Human Disease Resource: OMIM
DOID:0070043 - autosomal dominant non-syndromic intellectual disability 13 |
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DOID:0070043 - autosomal dominant non-syndromic intellectual disability 13 |