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EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS

Term:Unclassified primitive or secondary maculopathy
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Accession:EFO:Orphanet:98666 term browser browse the term


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Term paths to the root
Path 1
Term Annotations click to browse term
  experimental factor 0
    material property 0
      disposition 0
        disease 0
          genetic disorder 0
            Rare genetic eye disease 0
              Genetic vitreous-retinal disease 0
                Unclassified primitive or secondary maculopathy 0
                  Albers-Schönberg osteopetrosis 0
                  CLN1 disease 0
                  CLN11 disease 0
                  CLN13 disease 0
                  CLN2 disease 0
                  CLN3 disease 0
                  CLN4A disease 0
                  CLN4B disease 0
                  CLN5 disease 0
                  CLN6 disease 0
                  CLN7 disease 0
                  CLN8 disease 0
                  CLN9 disease 0
                  Cone rod dystrophy + 0
                  Congenital neuronal ceroid lipofuscinosis + 0
                  Cystoid macular dystrophy 0
                  Foveal hypoplasia - presenile cataract 0
                  Hermansky-Pudlak syndrome with neutropenia 0
                  Hypotrichosis with juvenile macular degeneration 0
                  Juvenile nephropathic cystinosis 0
                  Progressive epilepsy - intellectual disability, Finnish type 0
                  Sjögren-Larsson syndrome 0
                  Sorsby's fundus dystrophy 0
                  Zellweger syndrome 0
                  neuronal ceroid-lipofuscinosis, dominant/recessive 0
Path 2
Term Annotations click to browse term
  experimental factor 0
    material property 0
      disposition 0
        disease 0
          head and neck disorder 0
            disease of orbital region 0
              eye disease 0
                Rare genetic eye disease 0
                  Genetic vitreous-retinal disease 0
                    Unclassified primitive or secondary maculopathy 0
                      Albers-Schönberg osteopetrosis 0
                      CLN1 disease 0
                      CLN11 disease 0
                      CLN13 disease 0
                      CLN2 disease 0
                      CLN3 disease 0
                      CLN4A disease 0
                      CLN4B disease 0
                      CLN5 disease 0
                      CLN6 disease 0
                      CLN7 disease 0
                      CLN8 disease 0
                      CLN9 disease 0
                      Cone rod dystrophy + 0
                      Congenital neuronal ceroid lipofuscinosis + 0
                      Cystoid macular dystrophy 0
                      Foveal hypoplasia - presenile cataract 0
                      Hermansky-Pudlak syndrome with neutropenia 0
                      Hypotrichosis with juvenile macular degeneration 0
                      Juvenile nephropathic cystinosis 0
                      Progressive epilepsy - intellectual disability, Finnish type 0
                      Sjögren-Larsson syndrome 0
                      Sorsby's fundus dystrophy 0
                      Zellweger syndrome 0
                      neuronal ceroid-lipofuscinosis, dominant/recessive 0
paths to the root