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Results 1 - 10 of 446 for WHO
  1. Clopidogrel resistance 
    ... clopidogrel is less effective than normal in people who are treated with it. Clopidogrel (also known as ... small thin tube (stent).People with clopidogrel resistance who receive clopidogrel are at risk of serious, sometimes ...
    https://medlineplus.gov/genetics/condition/clopidogrel-resistance - Genetics
  2. Non-alcoholic fatty liver disease 
    ... by alcohol abuse, but that occurs in people who do not drink heavily. The liver is a ...
    https://medlineplus.gov/.../non-alcoholic-fatty-liver-disease - Genetics
  3. Danon disease 
    ... efficiently. About half of people with Danon disease who have two X chromosomes have hypertrophic cardiomyopathy, and ... myopathy occurs in most people with Danon disease who have one Y chromosome and in some affected ...
    https://medlineplus.gov/genetics/condition/danon-disease - Genetics
  4. Kidney stones 
    ... shows that 35 to 50 percent of people who have one kidney stone will develop additional stones, ... other substances that cause stone development in individuals who have a history of kidney stones. Additionally, people ...
    https://medlineplus.gov/genetics/condition/kidney-stones - Genetics
  5. Duchenne and Becker muscular dystrophy 
    ... one of the two sex chromosomes. In males (who have only one X chromosome), one altered copy ... is sufficient to cause the condition. In females (who have two X chromosomes), a mutation would have ...
    https://medlineplus.gov/.../duchenne-and-becker-muscular-dystrophy - Genetics
  6. Christianson syndrome 
    ... coordination (ataxia), and difficulty standing or walking. Individuals who do learn to walk lose the ability in ... one of the two sex chromosomes. In males (who have only one X chromosome), one altered copy ...
    https://medlineplus.gov/genetics/condition/christianson-syndrome - Genetics
  7. Androgen insensitivity syndrome 
    ... affects 2 to 5 in 100,000 newborns who are assigned female at birth. Partial androgen insensitivity ... one of the two sex chromosomes. In individuals who have only one X chromosome (typical for males), ...
    https://medlineplus.gov/.../androgen-insensitivity-syndrome - Genetics
  8. Factor V Leiden thrombophilia 
    ... abnormal clots is also much higher in people who have a combination of the factor V Leiden ... gene. Additionally, the risk is increased in people who have the factor V Leiden mutation together with ...
    https://medlineplus.gov/.../condition/factor-v-leiden-thrombophilia - Genetics
  9. Lowe syndrome 
    ... one of the two sex chromosomes. In males (who have only one X chromosome), one altered copy ... is sufficient to cause the condition. In females (who have two X chromosomes), a mutation must be ...
    https://medlineplus.gov/genetics/condition/lowe-syndrome - Genetics
  10. Amyotrophic lateral sclerosis 
    ... development of ALS and FTD are related. Individuals who develop both conditions are diagnosed as having ALS- ... has one parent with the condition. Some people who inherit a familial genetic mutation known to cause ...
    https://medlineplus.gov/.../condition/amyotrophic-lateral-sclerosis - Genetics
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