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| Term | acrocephalosyndactylia | ID (Ontology) | DOID:12960 (Human Disease) |
| Definition | A synostosis that results_in craniosynostosis and syndactyly. | ||
| Also Known As | "Apert 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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dysostosis |__synostosis |__acrocephalosyndactylia 6 rec. |__Carpenter syndrome 2 rec. | |__Carpenter syndrome 1 1 rec. | |__Carpenter syndrome 2 1 rec. |__Greig cephalopolysyndactyly syndrome 1 rec. |__Pfeiffer syndrome 2 rec. |__Saethre-Chotzen syndrome 3 rec. |__Sakati-Nyhan syndrome |
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| Is a | synostosis | ||
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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ICD9CM:755.55 MESH:D000168 MIM:101200 NCI:C34348 SNOMEDCT_US_2023_03_01:63661009 UMLS_CUI:C1510455 |
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