Search Ontology:
Human Disease
autosomal dominant intellectual developmental disorder 65
- Term ID
- DOID:0061038
- Synonyms
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- Definition
- An autosomal dominant intellectual developmental disorder characterized by delayed motor and speech acquisition, variably impaired intellectual development, and behavioral abnormalities that has_material_basis_in heterozygous mutation in the KDM4B gene on chromosome 19p13. https://pubmed.ncbi.nlm.nih.gov/33232677/
- References
- Ontology
- Human Disease ( DOID:0061038 )
- is a type of
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Genes Involved
Zebrafish Models