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Results 1 - 10 of 19 for Renal atrophy
  1. What Is Mitochondrial Disease? (United Mitochondrial Disease Foundation)  
    Mitochondrial Diseases/Start Here ... Mitochondrial Diseases ... United Mitochondrial Disease Foundation
    https://umdf.org/what-is-mitochondrial-disease-2 - External Health Links
  2. Early Onset Scoliosis (Scoliosis Research Society)  
    Scoliosis/Teenagers ... Scoliosis ... Scoliosis Research Society ... Early Onset Scoliosis ... Early Onset Scoliosis refers to spine curvature presenting before 10 years ...
    https://www.srs.org/.../Conditions/Scoliosis/Early-Onset-Scoliosis - External Health Links
  3. Optic Nerve Disorders (National Library of Medicine)  
    The optic nerve is a bundle of more than 1 million nerve fibers that carry visual messages. You have one connecting the back of each eye (your retina) to ...
    https://medlineplus.gov/opticnervedisorders.html - Health Topics
  4. Patient support and advocacy groups 
    ... Familial Dysautonomia Now Foundation Families of Spinal Muscular Atrophy Fat Disorders Research Society Fetal Health Foundation Fibrous ... Foundation Soft Bones Spastic Paraplegia Foundation Spinal Muscular Atrophy UK Spondylitis Association of America Stennis Foundation Stevens- ...
    https://medlineplus.gov/about/general/genetics/supportadvocacygroups -
  5. Schimke immuno-osseous dysplasia 
    ... with Schimke immuno-osseous dysplasia often have kidney (renal) disease that may lead to life-threatening renal failure and end-stage renal disease (ESRD). Individuals ...
    https://medlineplus.gov/.../schimke-immuno-osseous-dysplasia - Genetics
  6. Familial dysautonomia 
    ... Tseng CH, Axelrod F. Prevalence and severity of renal disease in familial dysautonomia. Am J Kidney Dis. ... Kaufmann H. Developmental abnormalities, blood pressure variability and renal disease in Riley Day syndrome. J Hum Hypertens. ...
    https://medlineplus.gov/genetics/condition/familial-dysautonomia - Genetics
  7. CLPB deficiency 
    ... of calcium in the kidneys (nephrocalcinosis) or kidney (renal) cysts.Many people with mild, moderate, or severe ... Rahman S. Bi-allelic CLPB mutations cause cataract, renal cysts, nephrocalcinosis and 3-methylglutaconic aciduria, a novel ...
    https://medlineplus.gov/genetics/condition/clpb-deficiency - Genetics
  8. Williams Syndrome From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Developmental Disabilities/Specifics ... Developmental Disabilities ... Genetic Disorders/Specifics ... Genetic Disorders ... Genetic and Rare Diseases Information Center ...
    https://rarediseases.info.nih.gov/diseases/7891/williams-syndrome - External Health Links
  9. Carpal tunnel syndrome 
    ... type 1 diabetes, type 2 diabetes, hypothyroidism, kidney (renal) failure, transthyretin amyloidosis, and hereditary neuropathy with liability ...
    https://medlineplus.gov/genetics/condition/carpal-tunnel-syndrome - Genetics
  10. CLPB gene 
    ... Rahman S. Bi-allelic CLPB mutations cause cataract, renal cysts, nephrocalcinosis and 3-methylglutaconic aciduria, a novel ... CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder. Am ...
    https://medlineplus.gov/genetics/gene/clpb - Genetics
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