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General Information
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| Term |
Peters plus syndrome |
ID (Ontology) |
DOID:0080201 (Human Disease) |
| Definition |
A syndrome that is characterized by anterior chamber eye anomalies, short limbs with broad distal extremities, characteristic facial features, cleft lip/palate, and variable developmental delay/intellectual disability. |
| Also Known As |
"Krause-Kivlin syndrome" ; "Peters anomaly-short limb dwarfism syndrome" ; "Peters-plus syndrome" |
| 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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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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Peters plus syndrome | 1 | for disease ribbon | Peters plus syndrome | 1 | model of | Peters plus syndrome | 1 |
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Relationships