FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term autosomal dominant intellectual developmental disorder 39 ID (Ontology) DOID:0070069 (Human Disease)
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.
Also Known As "autosomal dominant mental retardation 39" ; "autosomal dominant non-syndromic intellectual disability 39" ; "MRD39"
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 Genes
 autosomal dominant intellectual developmental disorder 39       1
 for disease ribbon | autosomal dominant intellectual developmental disorder 39       1
 model of | autosomal dominant intellectual developmental disorder 39       1
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autosomal dominant disease__
intellectual disability_____|
                            autosomal dominant intellectual developmental disorder
                             |__autosomal dominant intellectual developmental disorder 39  1 rec.
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Is a autosomal dominant intellectual developmental disorder
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Synonyms
  • "autosomal dominant mental retardation 39" EXACT
    "autosomal dominant non-syndromic intellectual disability 39" EXACT
    "MRD39" EXACT OMO:0003012
Secondary IDs
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MIM:616521