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
  • NCI:C75463
  • OMIM:176270
  • 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
Citations
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.