Hereditary spherocytosis

CaLiGraph

Property	Value
rdf:type	owl:NamedIndividual Autosomal dominant disorder Cytoskeletal defect Hereditary hemolytic anemia ICD-9 codes 280–289: diseases of the blood and blood-forming organs
rdfs:label	Hereditary spherocytosis
owl:sameAs	dbr:Hereditary_spherocytosis
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Hematologic_disease http://en.wikipedia.org/wiki/Category:Autosomal_dominant_disorders http://en.wikipedia.org/wiki/Jaundice http://en.wikipedia.org/wiki/List_of_diseases_(H) http://en.wikipedia.org/wiki/Category:Cytoskeletal_defects http://en.wikipedia.org/wiki/Category:Hereditary_hemolytic_anemias http://en.wikipedia.org/wiki/Chronic_condition http://en.wikipedia.org/wiki/Congenital_hemolytic_anemia http://en.wikipedia.org/wiki/Spherocytosis http://en.wikipedia.org/wiki/List_of_ICD-9_codes_280%E2%80%93289:_diseases_of_the_blood_and_blood-forming_organs http://en.wikipedia.org/wiki/Anemia http://en.wikipedia.org/wiki/Genetic_disorder
skos:prefLabel	Hereditary spherocytosis
skos:altLabel	hereditary spherocytosis spherocytosis
clgo:eMedicineSubject	med
clgo:eMedicineTopic	2147
clgo:icd10	D58.0
clgo:icd9	282.0
clgo:medlinePlus	000530
clgo:meshId	D013103
clgo:omim	182900
clgo:orpha	822
is clgo:differentialDiagnosis of	Glucose-6-phosphate dehydrogenase deficiency

About: clgr:Hereditary_spherocytosis