Search Ontology:
Human Disease
autosomal dominant intellectual developmental disorder 62
- Term ID
- DOID:0061035
- Synonyms
-
- Definition
- An autosomal dominant intellectual developmental disorder that has_material_basis_in caused by heterozygous mutation in the DLG4 gene on chromosome 17p13. https://pubmed.ncbi.nlm.nih.gov/29460436/
- References
- Ontology
- Human Disease ( DOID:0061035 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models