This HTML5 document contains 78 embedded RDF statements represented using HTML+Microdata notation.

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PrefixNamespace IRI
n8http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C10)
n11http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C18)
n14http://caligraph.org/ontology/MeSH_code_(C18)
n7http://en.wikipedia.org/wiki/Category:
n12http://en.wikipedia.org/wiki/List_of_diseases_(T)
rdfshttp://www.w3.org/2000/01/rdf-schema#
skoshttp://www.w3.org/2004/02/skos/core#
n2http://caligraph.org/resource/Tay%E2%80%93
n9http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C16)
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
n13http://caligraph.org/ontology/MeSH_code_(C16)
n17http://dbpedia.org/resource/Tay%E2%80%93
clgohttp://caligraph.org/ontology/
n15http://caligraph.org/ontology/MeSH_code_(C10)
n4http://en.wikipedia.org/wiki/
provhttp://www.w3.org/ns/prov#
xsdhhttp://www.w3.org/2001/XMLSchema#
clgrhttp://caligraph.org/resource/
Subject Item
n2:Sachs_disease
rdf:type
clgo:Neurological_condition_or_disorder clgo:Autosomal_recessive_disorder clgo:Congenital_disorder clgo:Lipid_storage_disorder clgo:Childhood_disease_or_disorder n13: n14: clgo:Eponymous_disease clgo:Genetic_disorder clgo:Ashkenazi_Jews_topic clgo:Lysosomal_storage_disease n15: clgo:Neurological_disorder_in_children owl:NamedIndividual clgo:Neurodegenerative_disorder clgo:Rare_disease
rdfs:label
Tay–Sachs disease
owl:sameAs
n17:Sachs_disease
prov:wasDerivedFrom
n4:List_of_congenital_disorders n4:Chromosome_15 n7:Lipid_storage_disorders n4:Human_genome n4:Cherry-red_spot n8: n9: n11: n4:Degenerative_disease n7:Rare_diseases n4:Dysarthria n4:List_of_neurological_conditions_and_disorders n7:Neurological_disorders_in_children n12: n4:Race_and_health n4:GM_2_gangliosidosis n4:Sphingolipidoses n4:Hyperacusis n4:List_of_childhood_diseases_and_disorders n4:Medical_genetics_of_Jews n4:Macrocephaly n7:Autosomal_recessive_disorders n7:Congenital_disorders n7:Lysosomal_storage_diseases n4:Compound_heterozygosity n4:Dor_Yeshorim n4:Lysosomal_storage_disease n4:Genetic_disorder n7:Neurodegenerative_disorders n4:List_of_genetic_disorders n4:Prenatal_testing n4:Hypotonia n7:Ashkenazi_Jews_topics n4:List_of_eponymous_diseases
skos:prefLabel
Tay–Sachs disease
skos:altLabel
Tay–Sachs Tay-Sachs Tay-Sachs disease Tay-Sach's disease adult-onset Tay–Sachs Tay-Sachs diseases tay-sachs disease, ab
clgo:differentialDiagnosis
clgr:Sandhoff_disease clgr:Leigh_syndrome clgr:Neuronal_ceroid_lipofuscinosis
clgo:diseasesDB
12916
clgo:eMedicineSubject
ped
clgo:eMedicineTopic
3016
clgo:icd10
E75.0
clgo:icd9
330.1
clgo:medicalCause
clgr:Genetics
clgo:medicalDiagnosis
clgr:Genetic_testing clgr:Hexosaminidase
clgo:medlinePlus
001417
clgo:meshId
D013661
clgo:omim
272800
clgo:symptom
clgr:Hearing_loss clgr:Paralysis clgr:Seizure
clgo:treatment
clgr:Symptomatic_treatment