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General Information
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| Term |
Cenani-Lenz syndactyly syndrome |
ID (Ontology) |
DOID:0090015 (Human Disease) |
| Definition |
A dysostosis characterized by syndactyly, malformation of the forearm and lower limb bones, renal hypoplasia or aplasia and that has_material_basis_in homozygous or compound heterozygous mutation in the LRP4 gene on chromosome 11p11. |
| Also Known As |
"syndactyly type 7" |
| 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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Cenani-Lenz syndactyly syndrome | 2 | for disease ribbon | Cenani-Lenz syndactyly syndrome | 2 | model of | Cenani-Lenz syndactyly syndrome | 2 |
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