Fabry disease - CaLiGraph

Property	Value
rdf:type	Cardiogenetic disorder Systemic disease with ocular manifestations Lipid storage disorder owl:NamedIndividual Eponym Eponymous disease Neurological condition or disorder Rare disease Skin condition Lysosomal storage disease MeSH code (C10) MeSH code (C16) MeSH code (C18) X-linked recessive disorder Skin condition resulting from errors in metabolism
rdfs:label	Fabry disease
owl:sameAs	dbr:Fabry_disease
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Cardiomyopathy http://en.wikipedia.org/wiki/Fever_of_unknown_origin http://en.wikipedia.org/wiki/Mendelian_traits_in_humans http://en.wikipedia.org/wiki/Category:Rare_diseases http://en.wikipedia.org/wiki/List_of_diseases_(S) http://en.wikipedia.org/wiki/List_of_eponymous_diseases http://en.wikipedia.org/wiki/List_of_eponyms_(A%E2%80%93K) 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/Category:Lysosomal_storage_diseases http://en.wikipedia.org/wiki/Paresthesia http://en.wikipedia.org/wiki/Category:Cardiogenetic_disorders http://en.wikipedia.org/wiki/Restrictive_cardiomyopathy http://en.wikipedia.org/wiki/Human_genetics http://en.wikipedia.org/wiki/Sweat_gland http://en.wikipedia.org/wiki/Cataract http://en.wikipedia.org/wiki/Category:Lipid_storage_disorders http://en.wikipedia.org/wiki/Sphingolipidoses http://en.wikipedia.org/wiki/Sex_linkage http://en.wikipedia.org/wiki/Fever http://en.wikipedia.org/wiki/Category:X-linked_recessive_disorders 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/X-linked_recessive_inheritance http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C18) http://en.wikipedia.org/wiki/Category:Skin_conditions_resulting_from_errors_in_metabolism http://en.wikipedia.org/wiki/National_Society_of_Genetic_Counselors http://en.wikipedia.org/wiki/Inborn_error_of_lipid_metabolism http://en.wikipedia.org/wiki/List_of_systemic_diseases_with_ocular_manifestations http://en.wikipedia.org/wiki/Proteinuria http://en.wikipedia.org/wiki/Lysosomal_storage_disease
skos:prefLabel	Fabry disease
skos:altLabel	Anderson-Fabry disease Fabry Disease Fabry's disease Sweeley–Klionsky disease fabry disease
clgo:complications	Heart failure,abnormal heart rhythms
clgo:differentialDiagnosis	Hypertrophic cardiomyopathy
clgo:diseasesDB	4638
clgo:eMedicineSubject	neuro
clgo:eMedicineTopic	579
clgo:geneReviewsId	NBK1292
clgo:geneReviewsName	Fabry disease
clgo:icd10	E75.2 (ILDSE75.25)
clgo:icd9	272.7
clgo:medicalDiagnosis	Genetic testing
clgo:meshId	D000795
clgo:omim	301500
is clgo:medicalCause of	Hypertrophic cardiomyopathy

About: clgr:Fabry_disease