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500 Possible Causes for Oguchi Disease

  • Oguchi Disease Type 2

    , Oguchi Type 1 Oguchi Disease type 1 OGUCHI DISEASE 1 edit English Oguchi disease type 1 human disease Oguchi disease-1 CSNBO1 congenital stationary night blindness Oguchi[wikidata.org] Oguchi disease type 2 is a rare autosomal recessive form of congenital stationary night blindness.[ncbi.nlm.nih.gov] […] type 1 Night Blindness, Congenital Stationary, Oguchi Type 1 Oguchi Disease type 1 OGUCHI DISEASE 1 Statements Identifiers Sitelinks Wikipedia (4 entries) edit Wikibooks[wikidata.org]

  • Autosomal Dominant Congenital Stationary Night Blindness Type 2

    disease.[ncbi.nlm.nih.gov] , Oguchi Type 1 Oguchi Disease type 1 OGUCHI DISEASE 1 edit English Oguchi disease type 1 human disease Oguchi disease-1 CSNBO1 congenital stationary night blindness Oguchi[wikidata.org] […] called congenital stationary night blindness, Oguchi type 1 o … Wikipedia Oguchi disease — Ogu·chi disease (o gooґche) [Chuta Oguchi, Japanese ophthalmologist, 1875â “1945[translate.academic.ru]

  • Periodontitis

    Thorat Manojkumar, Garg Garima and Arjun Raju, Serum levels of oncostatin M (a gp 130 cytokine): an inflammatory biomarker in periodontal disease, Biomarkers, 15, 3, (277)[doi.org] Tao Zhang, Tomoko Kurita-Ochiai, Tomomi Hashizume, Sumito Oguchi, Yoshimitsu Abiko and Masafumi Yamamoto, Aggregatibacter actinomycetemcomitans Leads to Endothelial Apoptosis[doi.org]

  • Non-Syndromic Ocular Stickler Syndrome Type 1 

    Oguchi’s Disease Oguchi’s disease, another stationary form of congenital night blindness, is usually diagnosed by a combination of two readily observable phenomena.[entokey.com] Oguchi's disease: a. is an autosomal dominant condition b. is characterized by stationary night blindness c. is associated with colour blindness d. is characterized by Mizuo-Nakamura[mrcophth.com] Diseases With Selective Loss of b Wave Amplitude on ERG Testing X-linked juvenile retinoschisis Congenital stationary night blindness Oguchi’s disease Myotonic dystrophy Batten[medtextfree.wordpress.com]

  • Meniere's Disease

    Miyagawa M, Fukuoka H, Tsukada K, Oguchi T, Takumi Y, Sugiura M, et al. Endolymphatic hydrops and therapeutic effects are visualized in ‘atypical’ Meniere’s disease.[doi.org] ’ Meniere’s disease.[doi.org] Miyagawa M, Fukuoka H, Tsukada K, Oguchi T, Takumi Y, Sugiura M, Ueda H, Kadoya M, Usami S.[ncbi.nlm.nih.gov]

  • Familial Benign Flecked Retina

    disease Oligocone trichromacy Patterned dystrophy of the retinal pigment epithelium Pigmented paravenous retinochoroidal atrophy Progressive bifocal chorioretinal atrophy[se-atlas.de] disease Ophthalmoplegia, isolated, MT-TN related Optic atrophy Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy Patterned dystrophy[qlinics.com] Bothnia retinal dystrophy, Fundus albipunctatus, Newfoundland rod-cone dystrophy, Retinitis punctata albescens RPE65 Leber congenital amaurosis, Retinitis pigmentosa SAG Oguchi[genda.com.ar]

  • Alzheimer Disease

    Loss of astrocyte polarization in the tg-ArcSwe mouse model of Alzheimer's disease.[ncbi.nlm.nih.gov] J Exp Med. 2014; 211 :387–393. doi: 10.1084/jem.20131685. [ PMC free article ] [ PubMed ] [ CrossRef ] [ Google Scholar ] Yang J, Lunde LK, Nuntagij P, Oguchi T, Camassa LM[ncbi.nlm.nih.gov]

  • Fleck Retina of Kandori

    DISEASE 2 Oguchi disease is a rare autosomal recessive form of congenital stationary night blindness in which all other visual functions, including visual acuity, visual[mendelian.co] disease Fundus Albipunctatus.[umassmed.edu] disease Oligocone trichromacy Patterned dystrophy of the retinal pigment epithelium Pigmented paravenous retinochoroidal atrophy Primary ciliary dyskinesia-retinitis pigmentosa[se-atlas.de]

  • Myocardial Infarction

    Thorat Manojkumar, Garg Garima and Arjun Raju, Serum levels of oncostatin M (a gp 130 cytokine): an inflammatory biomarker in periodontal disease, Biomarkers, 15, 3, (277)[dx.doi.org] Crossref, Google Scholar 151 Koizumi Y, Kurita-Ochiai T, Oguchi S, Yamamoto M.[doi.org] Tao Zhang, Tomoko Kurita-Ochiai, Tomomi Hashizume, Sumito Oguchi, Yoshimitsu Abiko and Masafumi Yamamoto, Aggregatibacter actinomycetemcomitans Leads to Endothelial Apoptosis[dx.doi.org]

  • Bothnia Retinal Dystrophy

    […] and pineal gland (arrestin) S-AG ARRESTIN DKFZp686D1084 S-arrestin DKFZp686I1383 2 468#Rhodopsin phototransduction cascade in retina - the key role of Ca2 transport 181031#Oguchi[gedi.ci.uchicago.edu] disease Ophthalmoplegia, isolated, MT-TN related Optic atrophy Optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy Patterned dystrophy[qlinics.com] disease Oligocone trichromacy Optic atrophy-intellectual disability syndrome Optic nerve edema-splenomegaly syndrome PEHO syndrome Patterned dystrophy of the retinal pigment[se-atlas.de]

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