Search Ontology:
Human Disease

autosomal dominant intellectual developmental disorder 59

Term ID
DOID:0061033
Synonyms
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the CAMK2G gene on chromosome 10q22. https://pubmed.ncbi.nlm.nih.gov/30184290/
References
Ontology
Human Disease   ( DOID:0061033 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models