Visualize Submit Comment
Metadata
ID DOID:0080235
Name autosomal dominant mental retardation 48
Definition An autosomal dominant non-syndromic intellectual disability that has_material_basis_in heterozygous mutation in the RAC1 gene on chromosome 7p22.
https://pubmed.ncbi.nlm.nih.gov/28886345/
Xrefs

OMIM:617751

Parent Relationships

is_a autosomal dominant non-syndromic intellectual disability

Add an item to the term tracker