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Human Disease

autosomal dominant intellectual developmental disorder 39

Term ID
DOID:0070069
Synonyms
  • autosomal dominant mental retardation 39
  • autosomal dominant non-syndromic intellectual disability 39
  • MRD39
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
References
Ontology
Human Disease   ( DOID:0070069 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models