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| Term | congenital diaphragmatic hernia | ID (Ontology) | DOID:3827 (Human Disease) |
| Definition | A diaphragm disease characterized by the lack of development of all or part of the diaphragm, which results in an abnormal opening that allows the stomach and intestines to move into the chest cavity and crowd the heart and lungs. | ||
| Also Known As | "Diaphragmatic Hernia" | ||
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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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muscular disease |__diaphragm disease__ disease | |__physical disorder__| congenital diaphragmatic hernia 1 rec. |
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| Is a |
physical disorder diaphragm disease |
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GARD:1481 ICD10CM:K44 MESH:D006548 MIM:142340 MIM:222400 MIM:610187 NCI:C34687 ORDO:2140 SNOMEDCT_US_2023_03_01:155748004 UMLS_CUI:C0019284 |
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