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Results 1 - 10 of 1,313 for MedlinePlus
  1. 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
  2. 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
  3. SUCLG1-related mitochondrial DNA depletion syndrome 
    SUCLG1-related mitochondrial DNA (mtDNA) depletion syndrome is an inherited disorder that affects the early development of the brain. Signs and symptoms typically ...
    https://medlineplus.gov/...ated-mitochondrial-dna-depletion-syndrome - Genetics
  4. Stickler syndrome 
    Stickler syndrome is a group of hereditary conditions that are characterized by a distinctive facial appearance, eye abnormalities, hearing loss, and joint problems. ...
    https://medlineplus.gov/genetics/condition/stickler-syndrome - Genetics
  5. 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
  6. 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
  7. 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
  8. 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
  9. Glutathione synthetase deficiency 
    Glutathione synthetase deficiency is a disorder that prevents the production of an important molecule called glutathione. Glutathione helps prevent damage to cells ...
    https://medlineplus.gov/.../glutathione-synthetase-deficiency - Genetics
  10. 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
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