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MIM:616078 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 29; MRD29
Xenbase Genes: setbp1
Human Disease Resource: MIM
| MONDO:0014482 - intellectual disability, autosomal dominant 29 |
| MONDO:0018574 - obsolete intellectual disability-expressive aphasia-facial dysmorphism syndrome |
| DOID:0070059 - autosomal dominant intellectual developmental disorder 29 |
