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| Term | Prader-Willi syndrome | ID (Ontology) | DOID:11983 (Human Disease) |
| Definition | A chromosomal disease that is characterized by weak muscle tone, feeding difficulties, poor growth, and delayed development. Beginning in childhood, affected individuals develop an insatiable appetite, which leads to chronic overeating and obesity. | ||
| Also Known As | "Prader Willi syndrome" | ||
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disease |__syndrome_____________ genetic disease | |__chromosomal disease__| Prader-Willi syndrome |
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chromosomal disease syndrome |
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GARD:5575 ICD10CM:Q87.11 ICD9CM:759.81 MESH:D011218 MIM:176270 NCI:C75463 ORDO:739 SNOMEDCT_US_2023_03_01:205794007 UMLS_CUI:C0032897 |
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