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DOID:11983 - Prader-Willi syndrome
Disease Ontology 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.
Synonyms: Prader Willi syndrome,
Xenbase Genes : herc2, mkrn3
MONDO:0008300 - Prader-Willi syndrome |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
chromosomal disease (is_a),
syndrome (is_a)