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Results 1 - 10 of 863 for "ClinicalTrials.Gov"
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  1. 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
  2. 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
  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. 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
  5. Familial atrial fibrillation 
    ... atrial fibrillation National Organization for Rare Disorders (NORD) ClinicalTrials.gov ATRIAL FIBRILLATION, FAMILIAL, 1; ATFB1 ATRIAL FIBRILLATION, FAMILIAL, ...
    https://medlineplus.gov/.../condition/familial-atrial-fibrillation - Genetics
  6. 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
  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. 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
  9. Paramyotonia congenita 
    ... Von Eulenburg National Organization for Rare Disorders (NORD) ClinicalTrials.gov PARAMYOTONIA CONGENITA; PMC PubMed Cavel-Greant D, Lehmann- ...
    https://medlineplus.gov/genetics/condition/paramyotonia-congenita - Genetics
  10. Allan-Herndon-Dudley syndrome 
    ... Dudley syndrome National Organization for Rare Disorders (NORD) ClinicalTrials.gov ALLAN-HERNDON-DUDLEY SYNDROME; AHDS PubMed Dumitrescu AM, ...
    https://medlineplus.gov/.../condition/allan-herndon-dudley-syndrome - Genetics
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