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  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. Familial cold autoinflammatory syndrome type 2 
    Familial cold autoinflammatory syndrome type 2 is a condition that causes episodes of fever, skin rash, and joint pain. These episodes can be triggered by exposure ...
    https://medlineplus.gov/...ial-cold-autoinflammatory-syndrome-type-2 - Genetics
  3. VEXAS syndrome 
    VEXAS syndrome is a disorder involving episodes of fever and abnormal inflammation. VEXAS is an acronym that stands for the technical terms of key descriptors ...
    https://medlineplus.gov/genetics/condition/vexas-syndrome - Genetics
  4. 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
  5. 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
  6. 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
  7. 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
  8. 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
  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. 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
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