OBO ID: DOID:0112026
Term Name: non-syndromic X-linked intellectual disability 99 Search Ontology:
Synonyms:
  • MRX99
  • X-linked mental retardation 99
Definition: A non-syndromic X-linked intellectual disability characterized by developmental delay, hypotonia, and variable behavioral abnormalities that has_material_basis_in hemizygous mutation in USP9X on chromosome Xp11.4. https://pubmed.ncbi.nlm.nih.gov/24607389/
References:
Ontology: Human Disease   (DOID:0112026)
OTHER non-syndromic X-linked intellectual disability 99 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
USP9X Intellectual developmental disorder, X-linked 99 300919
USP9Y Intellectual developmental disorder, X-linked 99 300919
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None