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Neurodegeneration with brain iron accumulation that has material basis in autosomal recessive inheritance of mutation in the C19orf12 gene on chromosome 19q12

Property Value
dbo:description
  • neurodegeneration with brain iron accumulation that has material basis in autosomal recessive inheritance of mutation in the C19orf12 gene on chromosome 19q12 (en)
dbo:diseasesDB
  • 35161
dbo:geneReviewsId
  • NBK185329
dbo:geneReviewsName
  • Mitochondrial Membrane Protein-Associated Neurodegeneration (en)
dbo:gradNum
  • 12569
dbo:icd10
  • G23.0
dbo:omim
  • 614298 (xsd:integer)
dbo:orpha
  • 289560
dbo:symptom
dbo:wikiPageWikiLink
dbp:causes
  • C19orf12 mutation (en)
dbp:diseasesdb
  • 35161 (xsd:integer)
dbp:field
  • Neurology (en)
dbp:frequency
  • 1 (xsd:integer)
dbp:gardnum
  • 12569 (xsd:integer)
dbp:genereviewsname
  • Mitochondrial Membrane Protein-Associated Neurodegeneration (en)
dbp:genereviewsnbk
  • NBK185329 (en)
dbp:icd
  • (en)
  • G23.0 (en)
dbp:name
  • Mitochondrial membrane protein-associated neurodegeneration (en)
dbp:omim
  • 614298 (xsd:integer)
dbp:orphanet
  • 289560 (xsd:integer)
dbp:symptoms
  • Dystonia, parkinsonism, dementia (en)
dbp:synonyms
  • Neurodegeneration with brain iron accumulation 4 (en)
dbp:types
  • Recessive, dominant (en)
dbp:wikiPageUsesTemplate
dct:subject
rdf:type
rdfs:label
  • Mitochondrial membrane protein-associated neurodegeneration (en)
owl:sameAs
prov:wasDerivedFrom
foaf:isPrimaryTopicOf
foaf:name
  • Mitochondrial membrane protein-associated neurodegeneration (en)
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