OBO ID: DOID:0080241
Term Name: syndromic X-linked mental retardation 35 Search Ontology:
Synonyms:
Definition: A syndromic X-linked intellectual disability that has_material_basis_in mutation in the RPL10 gene on chromosome Xq28. https://pubmed.ncbi.nlm.nih.gov/26290468/
References:
Ontology: Human Disease   ( DOID:0080241 )
OTHER syndromic X-linked mental retardation 35 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
RPL10 Intellectual developmental disorder, X-linked syndromic 35 300998
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None