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General Information
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| Term |
syndromic X-linked intellectual disability Pilorge type |
ID (Ontology) |
DOID:0070422 (Human Disease) |
| Definition |
A syndromic X-linked intellectual disability characterized by global developmental delay with variably impaired intellectual development, speech delay, and behavioral abnormalities including autism spectrum disorder that has_material_basis_in heterozygous or hemizygous mutation in the GLRA2 gene on chromosome Xp22. |
| Also Known As |
"MRXSP" |
| 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 | 3 | | 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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syndromic X-linked intellectual disability Pilorge type | 3 | 9 | 1 | for disease ribbon | syndromic X-linked intellectual disability Pilorge type | -- | 8 | -- | model of | syndromic X-linked intellectual disability Pilorge type | 3 | 8 | -- |
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Relationships