OBO ID: DOID:0060817
Term Name: syndromic X-linked intellectual disability 34 Search Ontology:
Synonyms:
  • macrocephaly-intellectual disability-left ventricular non compaction syndrome
  • mental retardation, X-linked, syndromic 34
  • MRXS34
  • MRXSML
  • syndromic X-linked mental retardation Mircsof-Langouet type
Definition: A syndromic X-linked intellectual disability characterized by delayed psychomotor development, intellectual disability, impaired speech, dysmorphic facial features, and mild structural brain abnormalities, including thickening of the corpus callosum that has_material_basis_in mutation in the NONO gene on chromosome Xq13. https://www.ncbi.nlm.nih.gov/pubmed/26571461
References:
Ontology: Human Disease   ( DOID:0060817 )
OTHER syndromic X-linked intellectual disability 34 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NONO Intellectual developmental disorder, X-linked syndromic 34
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None