Search Ontology:
Human Disease

Prader-Willi syndrome

Term ID
DOID:11983
Synonyms
  • Prader Willi syndrome
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)
References
  • 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
Ontology
Human Disease   ( DOID:11983 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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