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General Information
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| Term |
non-syndromic X-linked intellectual disability 1 |
ID (Ontology) |
DOID:0112038 (Human Disease) |
| Definition |
A non-syndromic X-linked intellectual disability characterized by moderate to severe intellectual disability in males and varying levels of intellectual disability in females that has_material_basis_in hemizygous or heterozygous mutation in the IQSEC2 gene on chromosome Xp11.22. |
| Also Known As |
"MRX1" ; "MRX18" ; "MRX78" (for all, see Synonyms field below) |
| Comment |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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No relevant records available
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Genes |
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non-syndromic X-linked intellectual disability 1 | 1 | for disease ribbon | non-syndromic X-linked intellectual disability 1 | 1 | model of | non-syndromic X-linked intellectual disability 1 | 1 |
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Relationships