Preferred Name |
Prader-Willi syndrome |
|
Synonyms |
Prader Willi syndrome |
|
Definitions |
OMIM mapping confirmed by DO. [SN]. 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. |
|
ID |
http://purl.obolibrary.org/obo/DOID_11983 |
|
comment |
OMIM mapping confirmed by DO. [SN]. |
|
database_cross_reference |
ICD10CM:Q87.11 OMIM:176270 UMLS_CUI:C0032897 MESH:D011218 ICD9CM:759.81 SNOMEDCT_US_2020_03_01:205794007 GARD:5575 NCI:C75463 ORDO:739 |
|
has exact synonym |
Prader Willi syndrome |
|
has_obo_namespace |
disease_ontology |
|
id |
DOID:11983 |
|
imported from | ||
in_subset | ||
label |
Prader-Willi syndrome |
|
notation |
DOID:11983 |
|
prefLabel |
Prader-Willi syndrome |
|
textual 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. |
|
subClassOf |
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