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EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS

Term:Genetic vitreous-retinal disease
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Accession:EFO:Orphanet:98657 term browser browse the term
Synonyms:external_ontology: has_disease_location EFO:UBERON:0000970


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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
                Amaurosis - hypertrichosis 0
                Autosomal recessive leukoencephalopathy with ischemic stroke-retinitis pigmentosa syndrome 0
                Best vitelliform macular dystrophy 0
                Bietti crystalline dystrophy 0
                Butterfly-shaped pigment dystrophy 0
                Cleft lip - retinopathy 0
                Color-vision disease + 0
                Ectopia lentis - chorioretinal dystrophy - myopia 0
                Familial drusen 0
                Familial exudative vitreoretinopathy 0
                Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome 0
                Hypogonadotropic hypogonadism - retinitis pigmentosa 0
                Microcornea-myopic chorioretinal atrophy-telecanthus syndrome 0
                Muscular atrophy - ataxia - retinitis pigmentosa - diabetes mellitus 0
                Osteochondrodysplatic nanism - deafness - retinitis pigmentosa 0
                Osteoporosis - pseudoglioma 0
                Polyneuropathy - hearing loss - ataxia - retinitis pigmentosa - cataract 0
                Primary ciliary dyskinesia - retinitis pigmentosa 0
                Progressive cone dystrophy 0
                Retinal degeneration - nanophthalmos - glaucoma 0
                Retinal vasculopathy and cerebral leukodystrophy + 0
                Retinitis pigmentosa - intellectual disability - deafness - hypogenitalism 0
                Spastic tetraplegia - retinitis pigmentosa - intellectual disability 0
                Unclassified familial retinal dystrophy + 0
                Unclassified primitive or secondary maculopathy + 0
                Xeroderma pigmentosum complementation group B 0
                Xeroderma pigmentosum complementation group D 0
                Xeroderma pigmentosum complementation group F 0
                Xeroderma pigmentosum complementation group G 0
                autosomal dominant retinitis pigmentosa 0
                autosomal recessive retinitis pigmentosa 0
                proliferative vitreoretinopathy 0
                vitreous detachment 0
                Åland Islands eye disease 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
                    Amaurosis - hypertrichosis 0
                    Autosomal recessive leukoencephalopathy with ischemic stroke-retinitis pigmentosa syndrome 0
                    Best vitelliform macular dystrophy 0
                    Bietti crystalline dystrophy 0
                    Butterfly-shaped pigment dystrophy 0
                    Cleft lip - retinopathy 0
                    Color-vision disease + 0
                    Ectopia lentis - chorioretinal dystrophy - myopia 0
                    Familial drusen 0
                    Familial exudative vitreoretinopathy 0
                    Foveal hypoplasia-optic nerve decussation defect-anterior segment dysgenesis syndrome 0
                    Hypogonadotropic hypogonadism - retinitis pigmentosa 0
                    Microcornea-myopic chorioretinal atrophy-telecanthus syndrome 0
                    Muscular atrophy - ataxia - retinitis pigmentosa - diabetes mellitus 0
                    Osteochondrodysplatic nanism - deafness - retinitis pigmentosa 0
                    Osteoporosis - pseudoglioma 0
                    Polyneuropathy - hearing loss - ataxia - retinitis pigmentosa - cataract 0
                    Primary ciliary dyskinesia - retinitis pigmentosa 0
                    Progressive cone dystrophy 0
                    Retinal degeneration - nanophthalmos - glaucoma 0
                    Retinal vasculopathy and cerebral leukodystrophy + 0
                    Retinitis pigmentosa - intellectual disability - deafness - hypogenitalism 0
                    Spastic tetraplegia - retinitis pigmentosa - intellectual disability 0
                    Unclassified familial retinal dystrophy + 0
                    Unclassified primitive or secondary maculopathy + 0
                    Xeroderma pigmentosum complementation group B 0
                    Xeroderma pigmentosum complementation group D 0
                    Xeroderma pigmentosum complementation group F 0
                    Xeroderma pigmentosum complementation group G 0
                    autosomal dominant retinitis pigmentosa 0
                    autosomal recessive retinitis pigmentosa 0
                    proliferative vitreoretinopathy 0
                    vitreous detachment 0
                    Åland Islands eye disease 0
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