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Results 41 - 50 of 51 for Congenital disorder of glycosylation
  1. Common Variable Immunodeficiency (CVID) From the National Institutes of Health (National Institute of Allergy and Infectious Diseases)  
    Immune System and Disorders/Specifics ... Immune System and Disorders ... National Institute of Allergy and Infectious Diseases ... NIAID researches common variable ...
    https://www.niaid.nih.gov/.../common-variable-immunodeficiency-cvid - External Health Links
  2. Hyper-Immunoglobulin E Syndromes (HIES) From the National Institutes of Health (National Institute of Allergy and Infectious Diseases)  
    Immune System and Disorders/Specifics ... Immune System and Disorders ... National Institute of Allergy and Infectious Diseases ... From the National Institutes of Health
    https://www.niaid.nih.gov/.../hyper-immunoglobulin-e-syndromes-hies - External Health Links
  3. Primary Immune Deficiency Disease Genetics and Inheritance From the National Institutes of Health (National Institute of Allergy and Infectious Diseases)  
    Immune System and Disorders/Genetics ... Immune System and Disorders ... National Institute of Allergy and Infectious Diseases ... From the National Institutes of Health
    https://www.niaid.nih.gov/.../pidds-genetics-inheritance - External Health Links
  4. Primary Immune Deficiency Diseases (PIDDs) From the National Institutes of Health (National Institute of Allergy and Infectious Diseases)  
    Immune System and Disorders/Start Here ... Immune System and Disorders ... National Institute of Allergy and Infectious Diseases ... From the National Institutes of ...
    https://www.niaid.nih.gov/...rimary-immune-deficiency-diseases-pidds - External Health Links
  5. CRPPA gene 
    ... the most severe form of a group of disorders known as congenital muscular ... the normal glycosylation of α-dystroglycan. As a result, α-dystroglycan ...
    https://medlineplus.gov/genetics/gene/crppa - Genetics
  6. LARGE1 gene 
    ... the most severe form of a group of disorders known as congenital muscular ... the normal glycosylation of α-dystroglycan. As a result, α-dystroglycan ...
    https://medlineplus.gov/genetics/gene/large1 - Genetics
  7. POMT2 gene 
    ... dystrophy (also known as MDDGB2). Muscle-eye-brain disease is similar to ... As a result, glycosylation of α-dystroglycan is impaired. The severity of ...
    https://medlineplus.gov/genetics/gene/pomt2 - Genetics
  8. POMT1 gene 
    ... dystrophy (also known as MDDGB1). Muscle-eye-brain disease is similar to ... As a result, glycosylation of α-dystroglycan is impaired. The severity of ...
    https://medlineplus.gov/genetics/gene/pomt1 - Genetics
  9. FKRP gene 
    ... the most severe form of a group of disorders known as congenital muscular dystrophies. Walker-Warburg syndrome causes skeletal muscle ... found in a small number of people with congenital muscular dystrophy type 1C ... disease, which causes muscle weakness, eye problems, and intellectual ...
    https://medlineplus.gov/genetics/gene/fkrp - Genetics
  10. Walker-Warburg syndrome 
    ... congenital muscular dystrophy Genetic Testing Registry: Walker-Warburg congenital muscular dystrophy Walker-Warburg syndrome National Organization for Rare Disorders (NORD) ClinicalTrials.gov MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH ...
    https://medlineplus.gov/genetics/condition/walker-warburg-syndrome - Genetics
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