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| Term | Holzgreve-Wagner-Rehder Syndrome | ID (Ontology) | DOID:0060566 (Human Disease) |
| Definition | A syndrome characterized by Potter sequence, heart defect, cleft palate, polydactyly, and skeletal defects. | ||
| Also Known As | "Holzgreve syndrome" ; "Holzgreve Wagner Rehder Syndrome" | ||
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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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| Is a | syndrome | ||
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External Crossreferences & Linkouts
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MESH:C535327 MIM:236110 ORDO:2167 SNOMEDCT_US_2023_03_01:783159001 UMLS_CUI:C1856095 |
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