Angelman syndrome

genetic condition in humans

Wikidata entity: Q535364

Wikimedia Commons category is Angelman syndrome

P373 Commons category String Angelman syndrome ???
P61 discoverer or inventor ... Q705052 (Harry Angelman) Harry Angelman
P2888 exact match Url Ontology Lookup Service (OLS) ???
P2888 exact match Url Disease Ontology - Institute for Genome Sciences @ University of Maryland ???
P2888 exact match Url Ontology Lookup Service (OLS) ???
P1325 external data available at URL Url None ???
P2293 genetic association ... Q14878336 (UBE3A) UBE3A
P2293 genetic association ... Q18028997 (MECP2) MECP2
P1995 health specialty ... Q83042 (neurology) neurology
P1995 health specialty ... Q1071953 (medical genetics) medical genetics
P1692 ICD-9-CM String 759.89 ???
P31 instance of ... Q929833 (rare disease) rare disease
P31 instance of ... Q42303753 (designated intractable/rare disease) designated intractable/rare disease
P31 instance of ... Q55788864 (developmental defect during embryogenesis) developmental defect during embryogenesis
P31 instance of ... Q112193867 (class of disease) class of disease
P138 named after ... Q705052 (Harry Angelman) Harry Angelman
P1748 NCI Thesaurus ID String C75462 ???
P5008 on focus list of Wikimedia project ... Q4099686 (WikiProject Medicine) WikiProject Medicine
P279 subclass of ... Q12136 (disease) disease
P279 subclass of ... Q179630 (syndrome) syndrome
P279 subclass of ... Q360341 (organic brain syndrome) organic brain syndrome
P279 subclass of ... Q55785627 (chromosomal anomaly with epilepsy as a major feature) chromosomal anomaly with epilepsy as a major feature
P279 subclass of ... Q55785866 (genetic syndromic intellectual disability) genetic syndromic intellectual disability
P279 subclass of ... Q4501577 (chromosomal disease) chromosomal disease
P575 time of discovery or invention ... 1965-01-01 ???
External Ids
P268Bibliothèque nationale de France ID14597678q
P508BNCF Thesaurus ID48516
P1036Dewey Decimal Classification616.042
P1036Dewey Decimal Classification618.928588
P699Disease Ontology IDDOID:1932
P557DiseasesDB712
P1417Encyclopædia Britannica Online IDtopic/Angelman-syndrome
P646Freebase ID/m/0fbhc
P4317GARD rare disease ID5810
P668GeneReviews IDNBK1144
P7464Genetics Home Reference Conditions IDangelman-syndrome
P227GND ID4287555-9
P4229ICD-10-CMQ93.5
P7807ICD-11 ID (Foundation)1106558408
P7329ICD-11 ID (MMS)LD90.0
P493ICD-9 ID759.89
P3827JSTOR topic ID (archived)angelman-syndrome
P8408KBpedia IDAngelmanSyndrome
P665KEGG IDH01732
P244Library of Congress authority IDsh92000322
P604MedlinePlus ID007616
P604MedlinePlus ID007616
P486MeSH descriptor IDD017204
P672MeSH tree codeC10.228.662.075
P672MeSH tree codeC16.131.077.095
P672MeSH tree codeC16.131.260.040
P672MeSH tree codeC16.320.180.040
P672MeSH tree codeC16.320.447.250
P5270Mondo IDMONDO_0007113
P8189National Library of Israel J9U ID987007546505805171
P1368National Library of Latvia ID000352930
P7995NHS Health A to Z IDangelman-syndrome
P691NL CR AUT IDph938182
P492OMIM ID105830
P492OMIM ID105830
P10283OpenAlex IDC2778691456
P1550Orphanet ID72
P4233PatientsLikeMe condition IDangelman-syndrome
P3417Quora topic IDAngelman-Syndrome
P5082Store medisinske leksikon IDAngelmans_syndrom
P2892UMLS CUIC0162635
P11430UniProt disease IDDI-00121
P11143WikiProjectMed IDAngelman syndrome
P3471WikiSkripta article ID8492
P13591Yale LUX IDconcept/5c3cbd6d-91aa-4c2e-9001-36e709fbbbf2

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