non-syndromic X-linked intellectual developmental disorder 111

Term ID

DOID:0060929

Synonyms

• XLID111

Definition

A non-syndromic X-linked intellectual disability characterized by different degrees of impaired intellectual development associated with motor, speech and behavioral impairments that has_material_basis_in hemizygous or heterozygous mutation in the SLITRK2 gene on chromosome Xq27. https://pubmed.ncbi.nlm.nih.gov/35840571/

References

• OMIM:301107

Ontology

Human Disease   ( DOID:0060929 )