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General Information
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| Term |
Perry syndrome |
ID (Ontology) |
DOID:0060486 (Human Disease) |
| Definition |
A syndrome characterized by parkinsonism, hypoventilation, depression, and weight loss and that has_material_basis_in heterozygous mutation in the DCTN1 gene on chromosome 2p13. |
| Also Known As |
"parkinsonism with alveolar hypoventilation and mental depression" |
| 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 | 2 | | 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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Perry syndrome | 2 | 3 | 1 | ameliorates | Perry syndrome | 1 | -- | -- | for disease ribbon | Perry syndrome | -- | 2 | -- | model of | Perry syndrome | 1 | 2 | -- |
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Relationships