Hereditary elliptocytosis

CaLiGraph

Property	Value
rdf:type	owl:NamedIndividual Autosomal dominant disorder MeSH code (C16) Hereditary hemolytic anemia
rdfs:label	Hereditary elliptocytosis
owl:sameAs	dbr:Hereditary_elliptocytosis
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Hematologic_disease http://en.wikipedia.org/wiki/Neonatal_jaundice http://en.wikipedia.org/wiki/Category:Autosomal_dominant_disorders http://en.wikipedia.org/wiki/List_of_diseases_(H) http://en.wikipedia.org/wiki/Category:Hereditary_hemolytic_anemias http://en.wikipedia.org/wiki/Congenital_hemolytic_anemia http://en.wikipedia.org/wiki/Elliptocyte http://en.wikipedia.org/wiki/Asymptomatic http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C16) http://en.wikipedia.org/wiki/Anemia http://en.wikipedia.org/wiki/Hereditary_elliptocytosis
skos:prefLabel	Hereditary elliptocytosis
skos:altLabel	elliptocytosis hereditary elliptocytosis
clgo:diseasesDB	4172
clgo:eMedicineSubject	ped
clgo:eMedicineTopic	987
clgo:icd10	D58.1
clgo:icd9	282.1
clgo:medlinePlus	000563
clgo:meshId	D004612
clgo:omim	611804

About: clgr:Hereditary_elliptocytosis