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| Term | tetraamelia syndrome 1 | ID (Ontology) | DOID:0112192 (Human Disease) |
| Definition | A tetraamelia syndrome characterized by complete limb agenesis without defects of scapulae or clavicles that has_material_basis_in homozygous or compound heterozygous mutation in WNT3 on chromosome 17q21.31-q21.32. | ||
| Also Known As | "TETAMS1" ; "tetra-amelia syndrome 1" | ||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal recessive disease__ syndrome | |__tetraamelia syndrome_________| tetraamelia syndrome 1 3 rec. |
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| Is a |
autosomal recessive disease tetraamelia syndrome |
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External Crossreferences & Linkouts
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GARD:5148 MIM:273395 |
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