Intellectual disability, autosomal dominant 39

Definition

Any autosomal dominant non-syndromic intellectual disability in which the cause of the disease is a mutation in the MYT1L gene.

Also known as autosomal dominant intellectual disability 39, autosomal dominant non-syndromic intellectual disability caused by mutation in MYT1L, intellectual developmental disorder, autosomal dominant 39, intellectual disability, autosomal dominant 39, intellectual disability, autosomal dominant type 39, mental retardation, autosomal dominant type 39, MRD39, MYT1L autosomal dominant non-syndromic intellectual disability — per MONDO

Also identified as

• DOID 0070069 per MONDO
• OMIM 616521 per MONDO
• UMLS C4225296 per MONDO