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Human Disease

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
Ontology
Human Disease   ( DOID:0060929 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models