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ZIRC
OBO ID: DOID:11983
Term Name: Prader-Willi syndrome Search Ontology:
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. https://ghr.nlm.nih.gov/condition/prader-willi-syndrome
References:
  • CSP2005:1849-7731
  • GARD:5575
  • ICD10CM:Q87.1
  • ICD9CM:759.81
  • MESH:D011218
  • NCI:C75463
  • OMIM:176270
  • ORDO:739
  • SNOMEDCT_US_2018_03_01:89392001
  • UMLS_CUI:C0032897
Ontology: Human Disease   (DOID:11983)
OTHER Prader-Willi syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
NDN Prader-Willi syndrome 176270
SNRPN Prader-Willi syndrome 176270
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS (1)