Angelman syndrome - CaLiGraph

Property	Value
rdf:type	owl:NamedIndividual Eponymous disease Neurological condition or disorder Rare syndrome Skin condition Syndrome affecting the nervous system Genodermatose Learning disability Autosomal monosomy or deletion Congenital disorder Disorder causing seizures Fetal abnormality MeSH code (C10) MeSH code (C16) Genetic disorder
rdfs:label	Angelman syndrome
owl:sameAs	dbr:Angelman_syndrome
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Category:Learning_disabilities http://en.wikipedia.org/wiki/Category:Genodermatoses http://en.wikipedia.org/wiki/Karyotype http://en.wikipedia.org/wiki/Category:Autosomal_monosomies_and_deletions http://en.wikipedia.org/wiki/List_of_eponymous_diseases http://en.wikipedia.org/wiki/List_of_neurological_conditions_and_disorders http://en.wikipedia.org/wiki/List_of_skin_conditions http://en.wikipedia.org/wiki/List_of_syndromes http://en.wikipedia.org/wiki/List_of_genetic_disorders http://en.wikipedia.org/wiki/Epigenetics_of_human_development http://en.wikipedia.org/wiki/Hypopigmentation http://en.wikipedia.org/wiki/Category:Rare_syndromes http://en.wikipedia.org/wiki/Category:Syndromes_affecting_the_nervous_system http://en.wikipedia.org/wiki/Microdeletion_syndrome http://en.wikipedia.org/wiki/Ubiquitin http://en.wikipedia.org/wiki/SYNGAP1-related_intellectual_disability http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C10) http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C16) http://en.wikipedia.org/wiki/List_of_congenital_disorders http://en.wikipedia.org/wiki/List_of_fetal_abnormalities http://en.wikipedia.org/wiki/Category:Disorders_causing_seizures http://en.wikipedia.org/wiki/Aneuploidy
skos:prefLabel	Angelman syndrome
skos:altLabel	Angelman Angelman Syndrome Angelman syndrome (AS) Angelman_syndrome angelman syndrome
clgo:differentialDiagnosis	Prader–Willi syndrome Cerebral palsy Autism spectrum Rett syndrome
clgo:diseasesDB	712
clgo:geneReviewsId	NBK1144
clgo:geneReviewsName	Angelman Syndrome
clgo:icd10	Q93.5
clgo:icd9	759.89
clgo:medicalCause	Genetics
clgo:medicalDiagnosis	Genetic testing
clgo:medlinePlus	007616
clgo:meshId	D017204
clgo:omim	105830
clgo:orpha	72
clgo:symptom	Microcephaly Intellectual disability
clgo:treatment	Symptomatic treatment
is clgo:differentialDiagnosis of	1p36 deletion syndrome Mowat–Wilson syndrome

About: clgr:Angelman_syndrome