autosomal recessive intellectual developmental disorder 69

Term ID

DOID:0081230

Synonyms

• neurodevelopmental disorder with progressive movement abnormalities, cognitive decline, and brain abnormalities

Definition

An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation in the ZBTB11 gene on chromosome 3q12. https://pubmed.ncbi.nlm.nih.gov/29893856/

References

• MIM:618383

Ontology

Human Disease   ( DOID:0081230 )