OBO ID: DOID:0112048
Term Name: non-syndromic X-linked intellectual disability 101 Search Ontology:
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 MID2 on chromosome Xq22.3. https://pubmed.ncbi.nlm.nih.gov/24115387/
References:
Ontology: Human Disease   (DOID:0112048)
OTHER non-syndromic X-linked intellectual disability 101 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MID2 ?Intellectual developmental disorder, X-linked 101 300928
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None