Search Ontology:
Human Disease
autosomal dominant intellectual developmental disorder 58
- Term ID
- DOID:0061032
- Synonyms
-
- Definition
- An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the SET gene on chromosome 9q34. https://pubmed.ncbi.nlm.nih.gov/29688601/
- References
- Ontology
- Human Disease ( DOID:0061032 )
- is a type of
-
Other Pages
Genes Involved
Zebrafish Models