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Results 1 - 10 of 1,313 for MedlinePlus
  1. DLG4-related synaptopathy 
    DLG4-related synaptopathy is a condition that affects neurological development. This condition is characterized by delayed development and mild to moderate ...
    https://medlineplus.gov/genetics/condition/dlg4-related-synaptopathy - Genetics
  2. CUL3-related neurodevelopmental disorder 
    CUL3-related neurodevelopmental disorder is a condition that affects neurological and physical development. Children with CUL3-related neurodevelopmental ...
    https://medlineplus.gov/.../cul3-related-neurodevelopmental-disorder - Genetics
  3. Multiple familial trichoepithelioma 
    Multiple familial trichoepithelioma is a condition involving multiple skin tumors that develop from structures associated with the skin (skin appendages), such ...
    https://medlineplus.gov/.../multiple-familial-trichoepithelioma - Genetics
  4. Stickler syndrome 
    Stickler syndrome is a group of hereditary conditions characterized by a distinctive facial appearance, eye abnormalities, hearing loss, and joint problems. These ...
    https://medlineplus.gov/genetics/condition/stickler-syndrome - Genetics
  5. Hypertension 
    Hypertension is abnormally high blood pressure in the arteries, which are the blood vessels that carry blood from the heart to the rest of the body. As the heart ...
    https://medlineplus.gov/genetics/condition/hypertension - Genetics
  6. Neuropathy, ataxia, and retinitis pigmentosa 
    Neuropathy, ataxia, and retinitis pigmentosa (NARP) is a condition that causes a variety of signs and symptoms that mainly affect the nervous system. The condition ...
    https://medlineplus.gov/...europathy-ataxia-and-retinitis-pigmentosa - Genetics
  7. Ornithine translocase deficiency 
    Ornithine translocase deficiency is an inherited disorder that causes ammonia and other substances to build up (accumulate) in the blood. Ammonia, which is formed ...
    https://medlineplus.gov/.../ornithine-translocase-deficiency - Genetics
  8. Short QT syndrome 
    Short QT syndrome is a condition that can cause a disruption of the heart's normal rhythm (arrhythmia). In people with this condition, the heart (cardiac) muscle ...
    https://medlineplus.gov/genetics/condition/short-qt-syndrome - Genetics
  9. Familial atrial fibrillation 
    Familial atrial fibrillation is an inherited abnormality of the heart's normal rhythm. Atrial fibrillation is characterized by episodes of uncoordinated electrical ...
    https://medlineplus.gov/.../condition/familial-atrial-fibrillation - Genetics
  10. Hyperkalemic periodic paralysis 
    Hyperkalemic periodic paralysis is a condition that causes episodes of extreme muscle weakness or paralysis, usually beginning in infancy or early childhood. Most ...
    https://medlineplus.gov/.../hyperkalemic-periodic-paralysis - Genetics
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