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Results 1 - 10 of 10 for "Hypertension," essential 1
  1. AGTR1 gene 
    ... Tests of AGTR1 PubMed ANGIOTENSIN II RECEPTOR, TYPE 1; AGTR1 HYPERTENSION, ESSENTIAL NCBI Gene ClinVar Ding W, Wang F, Fang ...
    https://medlineplus.gov/genetics/gene/agtr1 - Genetics
  2. AGT gene 
    ... LB. Genotype-phenotype analysis of angiotensinogen polymorphisms and essential hypertension: the importance of haplotypes. J Hypertens. 2010 Jan;28(1):65-75. doi: 10.1097/HJH.0b013e328332031a. Citation ...
    https://medlineplus.gov/genetics/gene/agt - Genetics
  3. SLC12A3 gene 
    ... role of the Gitelman's syndrome gene in essential hypertension. Endocr J. 2008 May;55(2):305-10. ...
    https://medlineplus.gov/genetics/gene/slc12a3 - Genetics
  4. CAV1 gene 
    ... tissue. In these cells, caveolae appear to be essential for the normal transport, processing, and storage of fats.Caveolin-1 is also found in many other parts of ...
    https://medlineplus.gov/genetics/gene/cav1 - Genetics
  5. NCF1 gene 
    ... not deleted have a higher risk of developing hypertension.People with only one copy of the NCF1 gene have reduced levels of the neutrophil cytosolic factor 1 protein, which decreases the activity of NOX and ...
    https://medlineplus.gov/genetics/gene/ncf1 - Genetics
  6. MEN1 gene 
    ... of bones, nausea and vomiting, high blood pressure (hypertension), weakness, and fatigue. Primary hyperparathyroidism is the most common sign of another condition called multiple endocrine neoplasia type 1 (described below); however, familial isolated hyperparathyroidism is diagnosed ...
    https://medlineplus.gov/genetics/gene/men1 - Genetics
  7. KCNJ1 gene 
    ... other genetic variants might increase the risk of high blood pressure. Changes in the KCNJ1 gene ... rectifier potassium channel 1 inward rectifier K(+) channel Kir1.1 inwardly rectifying ...
    https://medlineplus.gov/genetics/gene/kcnj1 - Genetics
  8. SLC12A1 gene 
    ... genetic variants might increase the risk of developing high blood pressure. Changes in the SLC12A1 ... member 1 solute carrier family 12 (sodium/potassium/chloride transporters), ...
    https://medlineplus.gov/genetics/gene/slc12a1 - Genetics
  9. RAF1 gene 
    ... raf proto-oncogene serine/threonine protein kinase Raf-1 RAF1_HUMAN Tests of RAF1 PubMed RAF1 PROTOONCOGENE, SERINE/THREONINE KINASE ; RAF1 NCBI Gene ClinVar Hopper RK, Feinstein JA, Manning MA, Benitz W, Hudgins L. Neonatal pulmonary arterial hypertension and Noonan syndrome: two fatal cases with a ...
    https://medlineplus.gov/genetics/gene/raf1 - Genetics
  10. KIF1B gene 
    ... produce an excess of hormones that cause dangerously high blood pressure. KIF1B gene mutations are associated with nonsyndromic pheochromocytoma, ... Charcot-Marie-Tooth disease. Neurogenetics. 2002 Mar;4(1):1-15. doi: 10.1007/s10048-002-0130- ...
    https://medlineplus.gov/genetics/gene/kif1b - Genetics