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| Term | Potter's syndrome | ID (Ontology) | DOID:12594 (Human Disease) |
| Definition | A renal agenesis characterized by the typical physical appearance and associated pulmonary hypoplasia of a newborn as a direct result of kidney failure, oligohydramnios and compression while in the uterus. | ||
| Also Known As | "Potter sequence" ; "Potter 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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kidney disease |__renal agenesis |__Potter's syndrome |
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| Is a | renal agenesis | ||
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External Crossreferences & Linkouts
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GARD:4462 ICD10CM:Q60.6 NCI:C40435 SNOMEDCT_US_2023_03_01:41962002 UMLS_CUI:C0178426 |
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