Search Ontology:
Human Disease
autosomal dominant intellectual developmental disorder 59
- Term ID
- DOID:0061033
- Synonyms
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- 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 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models