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| Term | Carpenter syndrome | ID (Ontology) | DOID:0060234 (Human Disease) |
| Definition | An acrocephalosyndactylia characterized by craniosynostosis, acrocephaly, obesity, syndactyly and polydactyly. | ||
| Also Known As | "acrocephalopolysyndactyly type II" | ||
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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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synostosis |__acrocephalosyndactylia |__Carpenter syndrome 2 rec. |__Carpenter syndrome 1 1 rec. |__Carpenter syndrome 2 1 rec. |
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| Is a | acrocephalosyndactylia | ||
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External Crossreferences & Linkouts
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GARD:6003 MESH:C563187 MIM:PS201000 NCI:C98873 ORDO:65759 SNOMEDCT_US_2023_03_01:403767009 UMLS_CUI:C1275078 |
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