Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 474 for Clinical Condition
  1. APOE gene 
    ... alleles can contribute to the pathogenesis of numerous clinical conditions including HSV-1 corneal disease. Exp Eye Res. ... Scheltens P. The effect of APOE genotype on clinical phenotype in Alzheimer disease. Neurology. 2006 Aug 8;67(3):526-7. ...
    https://medlineplus.gov/genetics/gene/apoe - Genetics
  2. TNNT2 gene 
    ... McKenna WJ. Hypertrophic cardiomyopathy: the genetic determinants of clinical disease expression. Nat Clin Pract Cardiovasc Med. 2008 Mar; ...
    https://medlineplus.gov/genetics/gene/tnnt2 - Genetics
  3. TNNI3 gene 
    ... McKenna WJ. Hypertrophic cardiomyopathy: the genetic determinants of clinical disease expression. Nat Clin Pract Cardiovasc Med. 2008 Mar; ...
    https://medlineplus.gov/genetics/gene/tnni3 - Genetics
  4. MYH7 gene 
    ... McKenna WJ. Hypertrophic cardiomyopathy: the genetic determinants of clinical disease expression. Nat Clin Pract Cardiovasc Med. 2008 Mar; ...
    https://medlineplus.gov/genetics/gene/myh7 - Genetics
  5. BTK gene 
    ... resulting in reduced B cell numbers but no clinical disease. Clin Exp Immunol. 2008 Apr;152(1):39- ...
    https://medlineplus.gov/genetics/gene/btk - Genetics
  6. MYBPC3 gene 
    ... McKenna WJ. Hypertrophic cardiomyopathy: the genetic determinants of clinical disease expression. Nat Clin Pract Cardiovasc Med. 2008 Mar; ...
    https://medlineplus.gov/genetics/gene/mybpc3 - Genetics
  7. SGCE gene 
    ... C, Ghezzi D, Garavaglia B. Myoclonus-dystonia syndrome: clinical presentation, disease course, and genetic features in 11 families. Mov ... and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of ... or Free article on PubMed Central
    https://medlineplus.gov/genetics/gene/sgce - Genetics
  8. STXBP1 gene 
    ... Abramov D, Guiberson NGL, Burre J. STXBP1 encephalopathies: Clinical spectrum, disease mechanisms, and therapeutic strategies. J Neurochem. 2021 Apr; ...
    https://medlineplus.gov/genetics/gene/stxbp1 - Genetics
  9. HEXB gene 
    ... B, Jinawath N, Wattanasirichaigoon D. Infantile onset Sandhoff disease: clinical manifestation and a novel common mutation in Thai patients. BMC Pediatr. 2021 Jan 7;21(1):22. doi: 10.1186/s12887-020-02481-3. Citation on PubMed
    https://medlineplus.gov/genetics/gene/hexb - Genetics
  10. AR gene 
    ... on PubMed Zajac JD, Fui MN. Kennedy's disease: clinical significance of tandem repeats in the androgen receptor. Adv Exp Med Biol. 2012;769:153-68. Citation on PubMed
    https://medlineplus.gov/genetics/gene/ar - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next