OBO ID: DOID:0070069
Term Name: autosomal dominant non-syndromic intellectual disability 39 Search Ontology:
Synonyms:
  • autosomal dominant mental retardation 39
  • MRD39
Definition: An autosomal dominant non-syndromic intellectual disability 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)
OTHER autosomal dominant non-syndromic intellectual disability 39 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MYT1L Mental retardation, autosomal dominant 39 616521
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None