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DO Term : Prader-Willi syndrome [DOID:11983] Disease Ontology

Namespace  disease_ontology Obsolete  false
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.
  • synonyms:
  • GARD:5575,
  • Prader Willi syndrome,
  • ICD9CM:759.81,
  • NCI:C75463,
  • SNOMEDCT_US_2023_03_01:205794007,
  • UMLS_CUI:C0032897,
  • 176270,
  • ORDO:739,
  • OMIM:176270,
  • MESH:D011218,
  • ICD10CM:Q87.11
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents