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75 Possible Causes for Atrophic Macular Disease

  • Acute Kidney Failure

    Lim -- Macular, papular, vesiculobullous, and pustular diseases / Neil J.[worldcat.org] Werth -- Eczemas, photodermatoses, papulosquamous (including fungal) diseases, and figurate erythemas / Henry W.[worldcat.org] Korman -- Urticaria, drug hypersensitivity rashes, nodules and tumors, and atrophic diseases / Madeleine Duvic -- Infectious, hyperpigmentation and hypopigmentation, regional[worldcat.org]

  • Acute Kidney Injury

    Lim -- Macular, papular, vesiculobullous, and pustular diseases / Neil J.[worldcat.org] Werth -- Eczemas, photodermatoses, papulosquamous (including fungal) diseases, and figurate erythemas / Henry W.[worldcat.org] Korman -- Urticaria, drug hypersensitivity rashes, nodules and tumors, and atrophic diseases / Madeleine Duvic -- Infectious, hyperpigmentation and hypopigmentation, regional[worldcat.org]

  • Macular Degeneration

    Macular degeneration occurs in either a dry (atrophic) or wet (exudative) form.[eschenbach.com] Currently, no proven therapies for atrophic disease are available, but several agents are being investigated in clinical trials.[ncbi.nlm.nih.gov] The majority of patients (over 80% of AMD cases) have the dry or atrophic type of macular degeneration.[eschenbach.com]

  • Sick Sinus Syndrome

    DEGENERATION, X-LINKED ATROPHIC Macular dystrophy, retinal, 2 Macular dystrophy, vitelliform, adult-onset Macular dystrophy, vitelliform, adult-onset Malignant hyperthermia[pentacorelab.hu] Malignant tumor of testis Malouf syndrome Mandibuloacral dysostosis Maple syrup urine disease Maple syrup urine disease, type 3 Marfan's syndrome Marie Unna congenital hypotrichosis[pentacorelab.hu] […] syndrome 2 Long QT syndrome 3 Long QT syndrome 5 Long QT syndrome 6 Long QT syndrome 9 Lowe syndrome Lung cancer Lymphangiomyomatosis Lynch syndrome I Lynch syndrome II MACULAR[pentacorelab.hu]

  • Retinitis Pigmentosa

    […] degeneration, X-linked atrophic, Retinitis pigmentosa 3 XL 79 218 RPGRIP1 Cone rod dystrophy, Leber congenital amaurosis AR 44 145 RS1 Retinoschisis XL 44 262 SAG Retinitis[blueprintgenetics.com] AR 45 181 RP2 Retinitis pigmentosa XL 26 118 RPE65 Retinitis pigmentosa, Leber congenital amaurosis AR 31 197 RPGR Retinitis pigmentosa, Cone-rod dystrophy, X-linked, 1, Macular[blueprintgenetics.com] […] pigmentosa, Oguchi disease AD/AR 6 15 SAMD11 Retinitis pigmentosa AR 2 5 SEMA4A Retinitis pigmentosa, Cone rod dystrophy AR 4 14 SLC7A14 Retinitis pigmentosa 68 AR 4 8 SNRNP200[blueprintgenetics.com]

  • Dilated Cardiomyopathy 1R

    DEGENERATION, X-LINKED ATROPHIC Macular dystrophy, retinal, 2 Macular dystrophy, vitelliform, adult-onset Macular dystrophy, vitelliform, adult-onset Malignant hyperthermia[pentacorelab.hu] Malignant tumor of testis Malouf syndrome Mandibuloacral dysostosis Maple syrup urine disease Maple syrup urine disease, type 3 Marfan's syndrome Marie Unna congenital hypotrichosis[pentacorelab.hu] […] syndrome 2 Long QT syndrome 3 Long QT syndrome 5 Long QT syndrome 6 Long QT syndrome 9 Lowe syndrome Lung cancer Lymphangiomyomatosis Lynch syndrome I Lynch syndrome II MACULAR[pentacorelab.hu]

  • Dilated Cardiomyopathy Type 2B

    DEGENERATION, X-LINKED ATROPHIC Macular dystrophy, retinal, 2 Macular dystrophy, vitelliform, adult-onset Macular dystrophy, vitelliform, adult-onset Malignant hyperthermia[pentacorelab.hu] Malignant tumor of testis Malouf syndrome Mandibuloacral dysostosis Maple syrup urine disease Maple syrup urine disease, type 3 Marfan's syndrome Marie Unna congenital hypotrichosis[pentacorelab.hu] […] syndrome 2 Long QT syndrome 3 Long QT syndrome 5 Long QT syndrome 6 Long QT syndrome 9 Lowe syndrome Lung cancer Lymphangiomyomatosis Lynch syndrome I Lynch syndrome II MACULAR[pentacorelab.hu]

  • Autosomal Dominant Rhegmatogenous Retinal Detachment

    Stargardt’s disease (atrophic macula) Goldmann–Favre disease Senile retinoschisis Retinitis pigmentosa AUTOSOMAL DOMINANT VITREORETINOCHOROIDOPATHY Autosomal dominant neovascular[medtextfree.wordpress.com] Autosomal dominant neovascular inflammatory vitreoretinopathy Retnitis pigmentosa Proliferative retinopathy Uveitis X-LINKED JUVENILE RETINOSCHISIS Cystoid macular edema[medtextfree.wordpress.com] […] type) Goldmann–Favre disease EROSIVE VITREORETINOPATHY Stickler’s syndrome Retinitis pigmentosa AUTOSOMAL DOMINANT NEOVASCULAR INFLAMMATORY VITREORETINOPATHY Goldmann–Favre disease[medtextfree.wordpress.com]

  • Macular Degeneration, Early Onset

    macular disease Clinical features from OMIM: 616118 MGI Mouse Phenotypes related to Macular Degeneration, Early-Onset: 47 # Description MGI Source Accession Score Top Affiliating[malacards.org] Stargardt disease is a form of macular degeneration found in young people, caused by a recessive gene.[macular.org] […] clinical synopsis from OMIM: 58 Head And Neck Eyes: decreased visual acuity choroidal neovascularization pigmentary changes of macula pigment epithelial atrophy of macula atrophic[malacards.org]

  • Dysautonomia

    DEGENERATION, X-LINKED ATROPHIC Macular dystrophy, retinal, 2 Macular dystrophy, vitelliform, adult-onset Macular dystrophy, vitelliform, adult-onset Malignant hyperthermia[pentacorelab.hu] Malignant tumor of testis Malouf syndrome Mandibuloacral dysostosis Maple syrup urine disease Maple syrup urine disease, type 3 Marfan's syndrome Marie Unna congenital hypotrichosis[pentacorelab.hu] […] syndrome 2 Long QT syndrome 3 Long QT syndrome 5 Long QT syndrome 6 Long QT syndrome 9 Lowe syndrome Lung cancer Lymphangiomyomatosis Lynch syndrome I Lynch syndrome II MACULAR[pentacorelab.hu]

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