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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

AttributesValues
type
subClassOf
label
  • amelogenesis imperfecta type 3C
described by
id
  • DOID:0111722
database_cross_reference
  • OMIM:618386
has_exact_synonym
  • AI3C
  • amelogenesis imperfecta type IIIC
  • autosomal recessive amelogenesis imperfecta hypocalcification type
has_obo_namespace
  • disease_ontology
http://purl.obolib...g/obo/IAO_0000115
  • An amelogenesis imperfecta type 3 that is characterized by hypocalcified enamel in both the primary and secondary dentition and that has_material_basis_in homozygous mutation in the RELT gene on chromosome 11q13.
is topic of
is annotatedSource of
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