Search Ontology:
Human Disease

autosomal dominant intellectual developmental disorder 21

Term ID
DOID:0070051
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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models