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Results 1 - 10 of 950 for E -Capsaicin
  1. Ataxia with vitamin E deficiency 
    Ataxia with vitamin E deficiency is a disorder that impairs the body's ability to use vitamin E obtained from the diet. Vitamin E is an antioxidant, which means ...
    https://medlineplus.gov/.../ataxia-with-vitamin-e-deficiency - Genetics
  2. DOCK8 immunodeficiency syndrome 
    ... levels of an immune system protein called immunoglobulin E (IgE) in the blood; the levels can be ... IgE recurrent infection syndrome, autosomal recessive Hyper immunoglobulin E syndrome, autosomal recessive Hyperimmunoglobulin E recurrent infection syndrome, ...
    https://medlineplus.gov/.../dock8-immunodeficiency-syndrome - Genetics
  3. Hereditary diffuse gastric cancer 
    ... for making a protein called epithelial cadherin or E-cadherin. This protein is found within the membrane ... line the surfaces and cavities of the body. E-cadherin helps neighboring cells stick to one another ( ...
    https://medlineplus.gov/.../hereditary-diffuse-gastric-cancer - Genetics
  4. X-linked chondrodysplasia punctata 1 
    ... pass X-linked traits to their sons. Arylsulfatase E deficiency CDPX1 Chondrodysplasia punctata 1, X-linked X- ... X-linked recessive chondrodysplasia punctata: spectrum of arylsulfatase E gene mutations and expanded clinical variability. Am J ...
    https://medlineplus.gov/.../x-linked-chondrodysplasia-punctata-1 - Genetics
  5. Trisomy 18 
    ... 18 syndrome Edwards syndrome Trisomy 18 syndrome Trisomy E syndrome Genetic Testing Registry: Complete trisomy 18 Trisomy ... Epub 2010 Sep 28. Citation on PubMed Petek E, Pertl B, Tschernigg M, Bauer M, Mayr J, ...
    https://medlineplus.gov/genetics/condition/trisomy-18 - Genetics
  6. SYNGAP1-related intellectual disability 
    ... Korenke GC, Borggraefe I, Hoffmann-Zacharska D, Szczepanik E, Rudzka-Dybala M, Yis U, Caglayan H, Isapof A, Marey I, Panagiotakaki E, Korff C, Rossier E, Riess A, Beck-Woedl ...
    https://medlineplus.gov/.../syngap1-related-intellectual-disability - Genetics
  7. Bartter syndrome 
    Bartter syndrome is a group of very similar kidney disorders that cause an imbalance of potassium, sodium, chloride, and related molecules in the body.In some ...
    https://medlineplus.gov/genetics/condition/bartter-syndrome - Genetics
  8. Familial focal epilepsy with variable foci 
    ... Citation on PubMed Baulac S, Ishida S, Marsan E, Miquel C, Biraben A, Nguyen DK, Nordli D, ... V, Vlaicu M, Daniau M, Bielle F, Andermann E, Andermann F, Leguern E, Chassoux F, Picard F. ...
    https://medlineplus.gov/...amilial-focal-epilepsy-with-variable-foci - Genetics
  9. Primary sclerosing cholangitis 
    ... on PubMed Central Karlsen TH, Franke A, Melum E, Kaser A, Hov JR, Balschun T, Lie BA, ... A, Vermeire S, Beuers U, Manns MP, Schrumpf E, Boberg KM, Schreiber S. Genome-wide association analysis ...
    https://medlineplus.gov/.../condition/primary-sclerosing-cholangitis - Genetics
  10. 1q21.1 microdeletion 
    ... T, Amato S, Geragthy MT, Innis JW, Obersztyn E, Nowakowska B, Rosengren SS, Bader PI, Grange DK, ... books/NBK52787/ Citation on PubMed Harvard C, Strong E, Mercier E, Colnaghi R, Alcantara D, Chow E, ...
    https://medlineplus.gov/genetics/condition/1q211-microdeletion - Genetics
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