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| General Information | |||
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| Term | ring chromosome syndrome | ID (Ontology) | DOID:0070620 (Human Disease) |
| Definition | A chromosomal disease that has_material_basis_in chromosome fusion into a ring or ring-like structure. Ring chromosome syndrome phenotypes are inherently variable. | ||
| Also Known As | "ring syndrome" | ||
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| DO.org | |||
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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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No relevant statements available
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genetic disease |__chromosomal disease |__ring chromosome syndrome |__ring chromosome 14 syndrome |__ring chromosome 20 syndrome |
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| Is a | chromosomal disease | ||
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External Crossreferences & Linkouts
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ICD10CM:Q93.2 MESH:D012303 ORDO:363203 UMLS_CUI:C0035639 |
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