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Results 1 - 10 of 864 for "ClinicalTrials.Gov"
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  1. Hypertension 
    ... Essential hypertension National Organization for Rare Disorders (NORD) ClinicalTrials.gov HYPERTENSION, ESSENTIAL HYPERTENSION, ESSENTIAL, SUSCEPTIBILITY TO, 2 HYPERTENSION, ...
    https://medlineplus.gov/genetics/condition/hypertension - Genetics
  2. VEXAS syndrome 
    ... syndrome VEXAS National Organization for Rare Disorders (NORD) ClinicalTrials.gov VEXAS SYNDROME; VEXAS PubMed Beck DB, Bodian DL, ...
    https://medlineplus.gov/genetics/condition/vexas-syndrome - Genetics
  3. Stickler syndrome 
    ... Stickler syndrome National Organization for Rare Disorders (NORD) ClinicalTrials.gov STICKLER SYNDROME, TYPE I; STL1 MARSHALL SYNDROME; MRSHS ...
    https://medlineplus.gov/genetics/condition/stickler-syndrome - Genetics
  4. Neuropathy, ataxia, and retinitis pigmentosa 
    ... NARP syndrome National Organization for Rare Disorders (NORD) ClinicalTrials.gov NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA PubMed Ball M, ...
    https://medlineplus.gov/...europathy-ataxia-and-retinitis-pigmentosa - Genetics
  5. Glutathione synthetase deficiency 
    ... synthetase deficiency National Organization for Rare Disorders (NORD) ClinicalTrials.gov GLUTATHIONE SYNTHETASE DEFICIENCY; GSSD GLUTATHIONE SYNTHETASE DEFICIENCY OF ...
    https://medlineplus.gov/.../glutathione-synthetase-deficiency - Genetics
  6. Hyperkalemic periodic paralysis 
    ... periodic paralysis National Organization for Rare Disorders (NORD) ClinicalTrials.gov HYPERKALEMIC PERIODIC PARALYSIS; HYPP PubMed Cannon SC. An ...
    https://medlineplus.gov/.../hyperkalemic-periodic-paralysis - Genetics
  7. Familial hypercholesterolemia 
    ... familial hypercholesterolemia National Organization for Rare Disorders (NORD) ClinicalTrials.gov HYPERCHOLESTEROLEMIA, FAMILIAL, 1; FHCL1 HYPERCHOLESTEROLEMIA, FAMILIAL, 2; FHCL2 ...
    https://medlineplus.gov/.../condition/familial-hypercholesterolemia - Genetics
  8. Ornithine translocase deficiency 
    ... homocitrullinuria syndrome National Organization for Rare Disorders (NORD) ClinicalTrials.gov HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME; HHHS PubMed Camacho JA, ...
    https://medlineplus.gov/.../ornithine-translocase-deficiency - Genetics
  9. Hyperprolinemia 
    ... type 2 National Organization for Rare Disorders (NORD) ClinicalTrials.gov HYPERPROLINEMIA, TYPE I; HYRPRO1 HYPERPROLINEMIA, TYPE II; HYRPRO2 ...
    https://medlineplus.gov/genetics/condition/hyperprolinemia - Genetics
  10. Short QT syndrome 
    ... type 3 National Organization for Rare Disorders (NORD) ClinicalTrials.gov SHORT QT SYNDROME 1; SQT1 SHORT QT SYNDROME ...
    https://medlineplus.gov/genetics/condition/short-qt-syndrome - Genetics
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