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Human Disease

autosomal dominant intellectual developmental disorder 65

Term ID
DOID:0061038
Synonyms
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 )
Relationships
is a type of
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Genes Involved
Zebrafish Models