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Prader-Willi Syndrome

Disease ID: disease_node_6283

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Dbxref	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
Subclassof	DOID_225, DOID_0080014
Data Source	DOID, MESH
Synonyms	Prader Willi syndrome
Mesh Id	D011218
Mesh Label	Prader-Willi Syndrome
Mesh Subclassof	D000096803, D009765, D008607, D025063, D000015
Doid Label	Prader-Willi syndrome
Doid Description	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. OMIM mapping confirmed by DO. [SN].
Disease Node Id	disease_node_6283
Doid Id	DOID_11983
Disease Has Basis In	SYMP_0000462
Label	Prader-Willi Syndrome

Outgoing r'ship SUBCLASS_OF to/from Syndrome(ID:disease_node_7213) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Chromosomal Disease(ID:disease_node_17149) (Disease)

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