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Human Disease

autosomal dominant intellectual developmental disorder 36

Term ID
DOID:0070066
Synonyms
  • autosomal dominant mental retardation 36
  • autosomal dominant non-syndromic intellectual disability 36
  • MRD36
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the PPP2R1A gene on chromosome 19q13.41. https://www.ncbi.nlm.nih.gov/pubmed/25533962
References
Ontology
Human Disease   ( DOID:0070066 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models