autosomal recessive intellectual developmental disorder 65

Term ID

DOID:0081226

Synonyms

Definition

An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous or compound heterozygous mutation in the KDM5B gene on chromosome 1q32. https://pubmed.ncbi.nlm.nih.gov/29276005/

References

• OMIM:618109

Ontology

Human Disease   ( DOID:0081226 )