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An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • Fanconi Syndrome
rdfs:subClassOf
Semantic_Type
  • Disease or Syndrome
Preferred_Name
  • Fanconi Syndrome
UMLS_CUI
  • C0015624
Legacy_Concept_Name
  • Fanconi_Syndrome
FULL_SYN
  • Lignac-Fanconi SyndromeSYNCI
  • Fanconi's syndromePTNCI-GLOSSCDR0000044357
  • Fanconi SyndromePTNCI
  • Fanconi SyndromeSYNCI
  • De Toni-Debre-Fanconi SyndromeSYNCI
DEFINITION
  • A genetic or acquired disorder characterized by impairment of the function of the proximal tubules of the kidney. It results in decreased reabsorption of electrolytes, glucose, amino acids, and other nutrients.NCI
code
  • C3034
is rdfs:subClassOf of
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