OBO ID: DOID:0112022
Term Name: non-syndromic X-linked intellectual disability 21 Search Ontology:
Synonyms:
  • MRX21
  • MRX34
  • X-linked mental retardation 21
  • X-linked mental retardation 21/34
  • X-linked mental retardation 34
Definition: A non-syndromic X-linked intellectual disability characterized by a spectrum of cognitive neurologic impairments ranging from moderate mental retardation to high-functioning autism that has_material_basis_in hemizygous mutation in IL1RAPL1 on chromosome Xp21.3-p21.2. https://pubmed.ncbi.nlm.nih.gov/18801879/
References:
Ontology: Human Disease   (DOID:0112022)
OTHER non-syndromic X-linked intellectual disability 21 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
IL1RAPL1 Intellectual developmental disorder, X-linked 21 300143
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None