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

• OMIM:616362

Ontology

Human Disease   ( DOID:0070066 )