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About:
clgr:
Pyruvate_kinase_deficiency
Property
Value
rdf:
type
owl:
NamedIndividual
Inborn error of carbohydrate metabolism
Hereditary hemolytic anemia
rdfs:
label
Pyruvate kinase deficiency
owl:
sameAs
dbr:
Pyruvate_kinase_deficiency
prov:
wasDerivedFrom
http://en.wikipedia.org/wiki/Hematologic_disease
http://en.wikipedia.org/wiki/Category:Inborn_errors_of_carbohydrate_metabolism
http://en.wikipedia.org/wiki/Echinocyte
http://en.wikipedia.org/wiki/Neonatal_jaundice
http://en.wikipedia.org/wiki/Jaundice
http://en.wikipedia.org/wiki/List_of_diseases_(P)
http://en.wikipedia.org/wiki/Methemoglobin
http://en.wikipedia.org/wiki/Category:Hereditary_hemolytic_anemias
http://en.wikipedia.org/wiki/Congenital_hemolytic_anemia
http://en.wikipedia.org/wiki/Hematopoietic_stem_cell_transplantation
skos:
prefLabel
Pyruvate kinase deficiency
skos:
altLabel
pyruvate kinase deficiency
clgo:
diseasesDB
11090
clgo:
eMedicineSubject
med
clgo:
eMedicineTopic
1980
clgo:
icd10
D55.2
clgo:
icd9
282.3
clgo:
medicalDiagnosis
Complete blood count
clgo:
medlinePlus
001197
clgo:
omim
266200
clgo:
symptom
Anemia
Tachycardia
clgo:
treatment
Blood transfusion
is
clgo:
differentialDiagnosis
of
Glucose-6-phosphate dehydrogenase deficiency