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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models