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General Information
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| Term |
non-syndromic X-linked intellectual disability 63 |
ID (Ontology) |
DOID:0112050 (Human Disease) |
| Definition |
A non-syndromic X-linked intellectual disability characterized by moderate to severe nonprogressive intellectual disability in males and moderate intellectual disability to normal intelligence in females that has_material_basis_in heterozygous mutation in the ACSL4 gene on chromosome Xq23. |
| Also Known As |
"ACSL4-related intellectual disability" ; "MRX63" ; "MRX68" (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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| Data Class | Field | Records |
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| Alleles (FBal) | HUMAN_DISEASE_INTERACTIONS | 8 | | Human Disease Models (FBhh) | DOID | 1 |
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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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| Alleles | Genes | Human Disease Models |
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non-syndromic X-linked intellectual disability 63 | 8 | 5 | 1 | ameliorates | non-syndromic X-linked intellectual disability 63 | 4 | -- | -- | for disease ribbon | non-syndromic X-linked intellectual disability 63 | -- | 1 | -- | model of | non-syndromic X-linked intellectual disability 63 | 5 | 1 | -- |
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Relationships