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Results 1 - 10 of 15 for World Health Organization
  1. PDGFRB-associated chronic eosinophilic leukemia 
    ... 1097/MOH.0b013e3283366c70. Citation on PubMed Gotlib J. World Health Organization-defined eosinophilic disorders: 2012 update on diagnosis, risk ...
    https://medlineplus.gov/...-associated-chronic-eosinophilic-leukemia - Genetics
  2. Erdheim-Chester disease 
    ... AD, Jaffe ES. The 2016 revision of the World Health Organization classification of lymphoid neoplasms. Blood. 2016 May 19; ...
    https://medlineplus.gov/genetics/condition/erdheim-chester-disease - Genetics
  3. Hereditary paraganglioma-pheochromocytoma 
    ... AS. Update from the 4th Edition of the World Health Organization Classification of Head and Neck Tumours: Paragangliomas. Head ...
    https://medlineplus.gov/...hereditary-paraganglioma-pheochromocytoma - Genetics
  4. GATA1 gene 
    ... A, Bloomfield CD. The 2008 revision of the World Health Organization (WHO) classification of myeloid neoplasms and acute leukemia: ...
    https://medlineplus.gov/genetics/gene/gata1 - Genetics
  5. Alpha thalassemia 
    ... haemoglobin disorders: an increasing global health problem. Bull World Health Organ. 2001;79(8):704-12. Epub 2001 ...
    https://medlineplus.gov/genetics/condition/alpha-thalassemia - Genetics
  6. Bipolar disorder 
    ... and correlates of bipolar spectrum disorder in the world mental health survey initiative. Arch Gen Psychiatry. 2011 Mar;68( ...
    https://medlineplus.gov/genetics/condition/bipolar-disorder - Genetics
  7. Alpha-1 antitrypsin deficiency 
    ... de Serres FJ, Blanco I, Fernandez-Bustillo E. Health implications of alpha1-antitrypsin deficiency in Sub-Sahara African countries and their emigrants in Europe and the New World. Genet Med. 2005 Mar;7(3):175-84. ...
    https://medlineplus.gov/.../condition/alpha-1-antitrypsin-deficiency - Genetics
  8. Complement component 2 deficiency 
    ... immune system difficulties, others do not have any health problems related to the disorder. In Western countries, complement component 2 deficiency is estimated to affect 1 in 20,000 individuals; its prevalence in other areas of the world is unknown. Complement component 2 deficiency is caused ...
    https://medlineplus.gov/.../complement-component-2-deficiency - Genetics
  9. Heterotaxy syndrome 
    ... Testing Registry: Heterotaxy, visceral, 6, autosomal Heterotaxia National Organization for Rare Disorders (NORD) ClinicalTrials.gov RIGHT ATRIAL ... Syndrome: Proceedings From the 10th International PCICS Meeting. World J Pediatr Congenit Heart Surg. 2015 Oct;6( ...
    https://medlineplus.gov/genetics/condition/heterotaxy-syndrome - Genetics
  10. Celiac disease 
    ... Genetic Testing Registry: Celiac disease Celiac disease National Organization for Rare Disorders (NORD) ClinicalTrials.gov CELIAC DISEASE, ... Risk factors in familial forms of celiac disease. World J Gastroenterol. 2010 Apr 21;16(15):1828- ...
    https://medlineplus.gov/genetics/condition/celiac-disease - Genetics
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