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General Information
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| Term |
syndromic X-linked intellectual disability Raymond type |
ID (Ontology) |
DOID:0060824 (Human Disease) |
| Definition |
A syndromic X-linked intellectual disability characterized by intellectual disability and marfanoid habitus that has_material_basis_in mutation in the ZDHHC9 gene on chromosome Xq26.1. |
| Also Known As |
"mental retardation, X-linked syndromic, Raymond type" ; "MRXSR" ; "X-linked syndromic intellectual developmental disorder Raymond type" |
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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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syndromic X-linked intellectual disability Raymond type | 1 | for disease ribbon | syndromic X-linked intellectual disability Raymond type | 1 | model of | syndromic X-linked intellectual disability Raymond type | 1 |
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Relationships