OBO ID: DOID:11983 |
Term Name: | Prader-Willi syndrome | Search Ontology: | |
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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. (2) | ||
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Ontology: | Human Disease ( DOID:11983 ) |
OTHER Prader-Willi syndrome PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS (1)
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