Search Ontology:
Human Disease

non-syndromic X-linked intellectual disability 101

Term ID
DOID:0112048
Synonyms
  • MRX101
  • X-linked mental retardation 101
Definition
A non-syndromic X-linked intellectual disability characterized by global developmental delay that has_material_basis_in hemizygous mutation in the MID2 gene on chromosome Xq22.3. https://pubmed.ncbi.nlm.nih.gov/24115387/
References
Ontology
Human Disease   ( DOID:0112048 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models