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Metadata
ID DOID:11983
Name 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, https://www.ncbi.nlm.nih.gov/books/NBK1330/
Xrefs

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

Subsets

DO_rare_slim

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Synonyms

Prader Willi syndrome [EXACT]

Parent Relationships

is_a syndrome

is_a chromosomal disease

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