autosomal recessive intellectual developmental disorder 78

Term ID

DOID:0061353

Synonyms

Definition

An autosomal recessive intellectual developmental disorder that is characterized by impaired intellectual development that is usually mild, but shows variable severity and that has_material_basis_in homozygous or compound heterozygous mutation in the WDR11 gene on chromosome 10q26.12. https://pubmed.ncbi.nlm.nih.gov/34413497/

References

• MIM:620237

Ontology

Human Disease   ( DOID:0061353 )