autosomal recessive intellectual developmental disorder 67

Term ID

DOID:0081228

Synonyms

Definition

An autosomal recessive intellectual developmental disorder that has_material_basis_in homozygous mutation or compound heterozygous mutation in the EIF3F gene on chromosome 11p15. https://pubmed.ncbi.nlm.nih.gov/30409806/

References

• OMIM:618295

Ontology

Human Disease   ( DOID:0081228 )