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Human Disease

autosomal dominant intellectual developmental disorder 41

Term ID
DOID:0070071
Synonyms
  • autosomal dominant mental retardation 41
  • autosomal dominant non-syndromic intellectual disability 41
  • MRD41
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the TBL1XR1 gene on chromosome 3q26.32. https://www.ncbi.nlm.nih.gov/pubmed/25102098
References
Ontology
Human Disease   ( DOID:0070071 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models