Metadata | |
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ID | DOID:0070069 |
Name | autosomal dominant intellectual developmental disorder 39 |
Definition | An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant heterozygous mutation in the MYT1L gene on chromosome 2p25.3. https://www.ncbi.nlm.nih.gov/pubmed/23033978 |
Xrefs | |
Synonyms |
autosomal dominant mental retardation 39 [EXACT] autosomal dominant non-syndromic intellectual disability 39 [EXACT] MRD39 [EXACT] |
Parent Relationships |