Search Ontology:
Human Disease

autosomal dominant intellectual developmental disorder 31

Term ID
DOID:0070061
Synonyms
  • autosomal dominant mental retardation 31
  • autosomal dominant non-syndromic intellectual disability 31
  • MRD31
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the PURA gene on chromosome 5q31.3. https://www.ncbi.nlm.nih.gov/pubmed/25439098
References
Ontology
Human Disease   ( DOID:0070061 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models
Citations