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| Term | fetal akinesia deformation sequence syndrome 2 | ID (Ontology) | DOID:0111378 (Human Disease) |
| Definition | A fetal akinesia deformation sequence that has_material_basis_in homozygous or compound heterozygous mutation in the RAPSN gene on chromosome 11p11.2. | ||
| Also Known As | "FADS2" | ||
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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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monogenic disease |__fetal akinesia deformation sequence syndrome__ autosomal genetic disease | |__autosomal recessive disease___________________| syndrome | |__fetal akinesia deformation sequence syndrome__| fetal akinesia deformation sequence syndrome 2 1 rec. |
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| Is a |
autosomal recessive disease fetal akinesia deformation sequence syndrome |
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| MIM:618388 | |||