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autosomal dominant non-syndromic intellectual disability (DOID:0060307)
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Synonyms: autosomal dominant mental retardation; autosomal dominant non-syndromic mental retardation
Alt IDs: OMIM:156200, OMIM:612337, OMIM:612580, OMIM:612581, OMIM:612621, OMIM:613443, OMIM:613970, OMIM:614104, OMIM:614113, OMIM:614254, OMIM:614255, OMIM:614256, OMIM:614257, OMIM:614563, OMIM:614607, OMIM:614608, OMIM:614609, OMIM:615009, OMIM:615074, OMIM:615075, OMIM:615502, OMIM:615761, OMIM:615828, OMIM:615873, ORDO:178469
Definition: A non-syndromic intellectual disability characterized by an autosomal dominant inheritance pattern.

Disease References using Mouse Models (3)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.11
The Jackson Laboratory