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Results 71 - 80 of 90 for Arterial disorder
  1. Craniofacial microsomia 
    ... medical attention. For reasons that are unclear, the disorder occurs about 50 percent more ... give rise to the muscles, arteries, nerves, and cartilage of the face and neck. ...
    https://medlineplus.gov/genetics/condition/craniofacial-microsomia - Genetics
  2. COL1A1 gene 
    ... mutation are prone to tearing (rupture) of major arteries in adulthood. The vascular type is associated with ... Health Condition Osteogenesis imperfecta is the most common disorder caused by mutations in the COL1A1 gene. People ...
    https://medlineplus.gov/genetics/gene/col1a1 - Genetics
  3. Preeclampsia 
    ... an insufficient connection between the placenta and the arteries of the uterus, the placenta does not get ... contribute to the risk of developing this complex disorder. These risk factors include a pregnancy with twins ...
    https://medlineplus.gov/genetics/condition/preeclampsia - Genetics
  4. Keratoconus 
    ... genetic syndromes, such as Leber congenital amaurosis and arterial tortuosity syndrome. When it is part of a ... in individuals with no family history of the disorder.The condition can also occur in families. In ...
    https://medlineplus.gov/genetics/condition/keratoconus - Genetics
  5. ABCG8 gene 
    ... body. These fatty substances build up in the arteries, skin, and other tissues, resulting in clogged blood ... levels, and sterol elimination: implications for classification and disease risk. J Lipid Res. 2011 Nov;52(11): ...
    https://medlineplus.gov/genetics/gene/abcg8 - Genetics
  6. Hereditary spherocytosis 
    ... flexible to travel from the large blood vessels (arteries) to the smaller blood vessels (capillaries). The proteins ... in each cell is sufficient to cause the disorder. In some cases, an affected person inherits the ...
    https://medlineplus.gov/genetics/condition/hereditary-spherocytosis - Genetics
  7. Hutchinson-Gilford progeria syndrome 
    ... Gilford progeria syndrome experience severe hardening of the arteries (arteriosclerosis) beginning in childhood. This condition greatly increases ... in each cell is sufficient to cause the disorder. The condition results from new mutations in the ...
    https://medlineplus.gov/.../hutchinson-gilford-progeria-syndrome - Genetics
  8. Familial atrial fibrillation 
    ... scar-like tissue in the lining of the arteries (atherosclerosis). Researchers are working to determine how a ... in each cell is sufficient to cause the disorder. In these cases, an affected person inherits the ...
    https://medlineplus.gov/.../condition/familial-atrial-fibrillation - Genetics
  9. NOTCH1 gene 
    ... of the heart (including the aorta and pulmonary artery). Still others involve a combination of these structural ... TAN-1 Tests of NOTCH1 PubMed AORTIC VALVE DISEASE 1; AOVD1 LEUKEMIA, CHRONIC LYMPHOCYTIC; CLL NOTCH RECEPTOR ...
    https://medlineplus.gov/genetics/gene/notch1 - Genetics
  10. Noonan syndrome with multiple lentigines 
    ... have heart problems have a narrowing of the artery from the heart to the lungs (pulmonary stenosis). ... syndrome with multiple lentigines National Organization for Rare Disorders (NORD) ClinicalTrials.gov LEOPARD SYNDROME 1; LPRD1 LEOPARD ...
    https://medlineplus.gov/.../noonan-syndrome-with-multiple-lentigines - Genetics
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