OBO ID: DOID:0112036 |
Term Name: | non-syndromic X-linked intellectual disability 105 | Search Ontology: | |
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Definition: | A non-syndromic X-linked intellectual disability characterized by borderline to moderate intellectual disability, variable poor or absent speech, and behavioral problems that has_material_basis_in hemizygous mutation in the USP27X gene on chromosome Xp11.23. https://pubmed.ncbi.nlm.nih.gov/25644381/ | ||
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Ontology: | Human Disease ( DOID:0112036 ) |
OTHER non-syndromic X-linked intellectual disability 105 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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USP27X | Intellectual developmental disorder, X-linked 105 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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