Search Ontology:
Human Disease

autosomal dominant intellectual developmental disorder 57

Term ID
DOID:0061031
Synonyms
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the TLK2 gene on chromosome 17q23. https://pubmed.ncbi.nlm.nih.gov/29861108/
References
Ontology
Human Disease   ( DOID:0061031 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models