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EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS

Term:eye degenerative disorder
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Accession:EFO:MONDO:0004884 term browser browse the term
Definition:A neurodegenerative disease that involves the eye.
Synonyms:exact_synonym: degenerative disorder of eye;   eye neurodegenerative disease;   eyeball of camera-type eye neurodegenerative disease;   neurodegenerative disease of eyeball of camera-type eye
 related_synonym: degenerative disorder of globe
 alt_id: MONDO:0004884
 xref: DOID:9799;   ICD10CM:H44.5;   ICD9:360.2;   ICD9:360.20;   ICD9:360.29;   ICD9:360.4;   ICD9:360.40;   MEDGEN:509655;   SCTID:62585004;   UMLS:C0154777


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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
          disorder of visual system 0
            eye disease 0
              eye degenerative disorder 0
                Alpers syndrome 0
                Ataxia - oculomotor apraxia type 1 0
                Ataxia with vitamin E deficiency 0
                Ataxia-telangiectasia 0
                Atypical progressive supranuclear palsy + 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
                Chédiak-Higashi syndrome 0
                Classical progressive supranuclear palsy 0
                Congenital neuronal ceroid lipofuscinosis + 0
                FLVCR1-related retinopathy with or without ataxia + 0
                Krabbe disease + 0
                Leber hereditary optic neuropathy 0
                Microphthalmia - brain atrophy 0
                Mohr-Tranebjaerg syndrome 0
                Progressive epilepsy - intellectual disability, Finnish type 0
                Refsum disease 0
                Sandhoff disease + 0
                Sjogren-Larsson syndrome 0
                Spastic paraplegia type 2 0
                Spinocerebellar ataxia with axonal neuropathy type 2 0
                Tay-Sachs disease + 0
                X-linked Charcot-Marie-Tooth disease type 5 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
                aceruloplasminemia 0
                autosomal dominant optic atrophy + 0
                autosomal recessive optic atrophy 0
                cerebrotendinous xanthomatosis 0
                choroidal sclerosis + 0
                corneal-cerebellar syndrome 0
                eyelid degenerative disorder + 0
                infantile cerebellar-retinal degeneration 0
                microphthalmia-brain atrophy syndrome 0
                multiple mitochondrial dysfunctions syndrome 4 0
                muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome 0
                neuromyelitis optica + 0
                neuronal ceroid-lipofuscinosis, dominant/recessive 0
                osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome 0
                peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain + 0
                rhizomelic chondrodysplasia punctata type 1 0
                spinocerebellar ataxia 27A 0
                tremor-ataxia-central hypomyelination syndrome 0
                vitreous syneresis + 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
                eye degenerative disorder 0
                  Alpers syndrome 0
                  Ataxia - oculomotor apraxia type 1 0
                  Ataxia with vitamin E deficiency 0
                  Ataxia-telangiectasia 0
                  Atypical progressive supranuclear palsy + 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
                  Chédiak-Higashi syndrome 0
                  Classical progressive supranuclear palsy 0
                  Congenital neuronal ceroid lipofuscinosis + 0
                  FLVCR1-related retinopathy with or without ataxia + 0
                  Krabbe disease + 0
                  Leber hereditary optic neuropathy 0
                  Microphthalmia - brain atrophy 0
                  Mohr-Tranebjaerg syndrome 0
                  Progressive epilepsy - intellectual disability, Finnish type 0
                  Refsum disease 0
                  Sandhoff disease + 0
                  Sjogren-Larsson syndrome 0
                  Spastic paraplegia type 2 0
                  Spinocerebellar ataxia with axonal neuropathy type 2 0
                  Tay-Sachs disease + 0
                  X-linked Charcot-Marie-Tooth disease type 5 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
                  aceruloplasminemia 0
                  autosomal dominant optic atrophy + 0
                  autosomal recessive optic atrophy 0
                  cerebrotendinous xanthomatosis 0
                  choroidal sclerosis + 0
                  corneal-cerebellar syndrome 0
                  eyelid degenerative disorder + 0
                  infantile cerebellar-retinal degeneration 0
                  microphthalmia-brain atrophy syndrome 0
                  multiple mitochondrial dysfunctions syndrome 4 0
                  muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome 0
                  neuromyelitis optica + 0
                  neuronal ceroid-lipofuscinosis, dominant/recessive 0
                  osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome 0
                  peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain + 0
                  rhizomelic chondrodysplasia punctata type 1 0
                  spinocerebellar ataxia 27A 0
                  tremor-ataxia-central hypomyelination syndrome 0
                  vitreous syneresis + 0
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