Search Ontology:
Human Disease

syndromic X-linked mental retardation 35

Term ID
DOID:0080241
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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models