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General Information
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| Term |
Stolerman neurodevelopmental syndrome |
ID (Ontology) |
DOID:0081443 (Human Disease) |
| Definition |
A syndrome that is characterized by developmental delay, often with motor and speech delay, mildly impaired intellectual development (in most patients), learning difficulties, and behavioral abnormalities, including autism spectrum disorder and that has_material_basis_in heterozygous mutation in the KDM6B gene on chromosome 17p13. |
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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 | 19 | | 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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Stolerman neurodevelopmental syndrome | 22 | 2 | 1 | for disease ribbon | Stolerman neurodevelopmental syndrome | -- | 1 | -- | model of | Stolerman neurodevelopmental syndrome | 19 | 1 | -- | DOES NOT model | Stolerman neurodevelopmental syndrome | 3 | -- | -- |
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Relationships