OBO ID: DOID:0070051
Term Name: autosomal dominant intellectual developmental disorder 21 Search Ontology:
Synonyms:
  • autosomal dominant mental retardation 21
  • autosomal dominant non-syndromic intellectual disability 21
  • MRD21
Definition: An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the CTCF gene on chromosome 16q22.1. https://www.ncbi.nlm.nih.gov/pubmed/23746550
References:
Ontology: Human Disease   ( DOID:0070051 )
OTHER autosomal dominant intellectual developmental disorder 21 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CTCF Intellectual developmental disorder, autosomal dominant 21 615502
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None