Prader–Willi syndrome

rare genetic disorder

Wikidata entity: Q594013









Wikimedia Commons category is Prader-Willi syndrome

P373 Commons category String Prader-Willi syndrome ???
P2176 drug or therapy used for treatment ... Q7559307 (somatrem) somatrem
P2888 exact match Url Ontology Lookup Service (OLS) ???
P2888 exact match Url Disease Ontology - Institute for Genome Sciences @ University of Maryland ???
P1325 external data available at URL Url None ???
P2293 genetic association ... Q18029889 (NDN) NDN
P2293 genetic association ... Q18031635 (SNRPN) SNRPN
P1995 health specialty ... Q83042 (neurology) neurology
P1995 health specialty ... Q123028 (pediatrics) pediatrics
P1995 health specialty ... Q1071953 (medical genetics) medical genetics
P1692 ICD-9-CM String 759.81 ???
P31 instance of ... Q929833 (rare disease) rare disease
P31 instance of ... Q42303753 (designated intractable/rare disease) designated intractable/rare disease
P31 instance of ... Q112193867 (class of disease) class of disease
P2716 montage image CommonsMedia http://commons.wikimedia.org/wiki/Special:FilePath/Pws.jpg ???
P138 named after ... Q118977 (Heinrich Willi) Heinrich Willi
P138 named after ... Q124502 (Andrea Prader) Andrea Prader
P1748 NCI Thesaurus ID String C75463 ???
P5008 on focus list of Wikimedia project ... Q4099686 (WikiProject Medicine) WikiProject Medicine
P5555 schematic CommonsMedia http://commons.wikimedia.org/wiki/Special:FilePath/Prader-Willi%20and%20Angelman%20Syndrome%20%28Homo%20sapiens%29.svg ???
P5555 schematic CommonsMedia http://commons.wikimedia.org/wiki/Special:FilePath/Pws.svg ???
P279 subclass of ... Q12136 (disease) disease
P279 subclass of ... Q179630 (syndrome) syndrome
P279 subclass of ... Q55786310 (syndromic obesity) syndromic obesity
P279 subclass of ... Q4501577 (chromosomal disease) chromosomal disease
P10 video CommonsMedia http://commons.wikimedia.org/wiki/Special:FilePath/Prader%20willi%20syndrome.webm ???
External Ids
P268Bibliothèque nationale de France ID12468434q
P508BNCF Thesaurus ID67274
P1036Dewey Decimal Classification616.042
P1036Dewey Decimal Classification618.920042
P699Disease Ontology IDDOID:11983
P557DiseasesDB10481
P673eMedicine ID947954
P1417Encyclopædia Britannica Online IDscience/Prader-Willi-syndrome
P646Freebase ID/m/0fb3f
P4317GARD rare disease ID5575
P668GeneReviews IDNBK1330
P7464Genetics Home Reference Conditions IDprader-willi-syndrome
P227GND ID4201277-6
P4229ICD-10-CMQ87.1
P7807ICD-11 ID (Foundation)393773440
P7329ICD-11 ID (MMS)LD90.3
P3827JSTOR topic ID (archived)prader-willi-syndrome
P665KEGG IDH00478
P244Library of Congress authority IDsh85106050
P604MedlinePlus ID001605
P604MedlinePlus ID001605
P486MeSH descriptor IDD011218
P672MeSH tree codeC10.597.606.360.690
P672MeSH tree codeC16.131.077.730
P672MeSH tree codeC16.131.260.700
P672MeSH tree codeC16.320.180.700
P672MeSH tree codeC16.320.447.500
P672MeSH tree codeC18.654.726.750.500.740
P8189National Library of Israel J9U ID987007531653205171
P349NDL Authority ID01179976
P7995NHS Health A to Z IDprader-willi-syndrome
P492OMIM ID176270
P492OMIM ID176270
P1550Orphanet ID739
P1461Patientplus IDprader-willi-syndrome-pro
P4233PatientsLikeMe condition IDprader-willi-syndrome
P3417Quora topic IDPrader-Willi-Syndrome
P5806SNOMED CT ID89392001
P5082Store medisinske leksikon IDPrader-Willis_syndrom
P2892UMLS CUIC0032897
P2892UMLS CUIC0265222
P12086WikiKids IDSyndroom_van_Prader-Willi
P11143WikiProjectMed IDPrader–Willi syndrome
P3471WikiSkripta article ID8491
P4839Wolfram Language entity codeEntity["Disease", {"ICDNine759.81", "Primary"}]
P13591Yale LUX IDconcept/20e85c46-b52a-49ce-a2c6-bb9c0b286d72
P2347YSO ID18144

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