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| Term | distal arthrogryposis type 10 | ID (Ontology) | DOID:0111593 (Human Disease) |
| Definition | A distal arthrogryposis that has_material_basis_in heterozygous mutation in the chromosome region 2q31.3-q32.1. | ||
| Also Known As | "DA10" ; "plantar flexion contracture" ; "short Achilles tendon" (for all, see Synonyms field below) | ||
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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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No relevant statements available
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autosomal genetic disease |__autosomal dominant disease__ muscle tissue disease | |__distal arthrogryposis_______| distal arthrogryposis type 10 |
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| Is a |
distal arthrogryposis autosomal dominant disease |
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External Crossreferences & Linkouts
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MESH:C566069 MIM:187370 ORDO:251515 |
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