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About:
metal metabolism disorder
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An Entity of Type :
http://wikiba.se/ontology#Item
, within Data Space :
wasabi.inria.fr
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Type:
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Attributes
Values
type
Item
label
metal metabolism disorder
preferred label
metal metabolism disorder
described by
https://covidontheweb.inria.fr:4443/about/id/entity/http/ns.inria.fr/covid19/graph/wikidata-named-entities-full
proxy:entity/http/ns.inria.fr/covid19/graph/wikidata-named-entities-full
proxy:entity/http/www.wikidata.org/entity/Q819207
schema:name
metal metabolism disorder
schema:description
inherited metabolic disorder that involves metabolic disturbances in the processing or distribution of dietary minerals
is
wdt:P279
of
pseudohypoparathyroidism
hemosiderosis
aceruloplasminemia
pulmonary hemosiderosis
Wilson disease
hypokalemic periodic paralysis
Iron overload
Menkes disease
Iron poisoning
HFE hereditary haemochromatosis
hyperkalemic periodic paralysis
acrodermatitis enteropathica
hemochromatosis type 2
periodic paralysis
Andersen-Tawil syndrome
Neonatal hemochromatosis
transfusion hemosiderosis
superficial siderosis of the central nervous system
African iron overload
Thyrotoxic periodic paralysis
Molybdenum cofactor deficiency
GRACILE syndrome
is
topic
of
pseudohypoparathyroidism
covid:graph/wikidata-named-entities-full
is
http://www.wikidat...op/statement/P279
of
wd:statement/Q819207-9EEE1921-01F9-444E-8EF5-283DEED4C697
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