| Metadata | |
|---|---|
| ID | DOID:0080234 |
| Name | Clark-Baraitser syndrome |
| Definition | An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the TRIP12 gene on chromosome 2q36. https://pubmed.ncbi.nlm.nih.gov/27848077/ |
| Xrefs | |
| Subsets |
DO_rare_slim |
| Synonyms |
autosomal dominant intellectual disability 49 [EXACT] autosomal dominant mental retardation 49 [EXACT] Baraitser syndrome [EXACT] CLABARS [EXACT] |
| Parent Relationships |