autosomal dominant intellectual developmental disorder 64

Term ID

DOID:0061037

Synonyms

Definition

An autosomal dominant intellectual developmental disorder characterized by mildly to severely impaired intellectual development (ID) with speech delays that has_material_basis_in heterozygous mutation in the ZNF292 gene on chromosome 6q14. https://pubmed.ncbi.nlm.nih.gov/31723249/

References

• MIM:619188

Ontology

Human Disease   ( DOID:0061037 )