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Results 31 - 40 of 674 for Protein S deficiency disease
  1. Learn about Alpha-1 Antitrypsin Deficiency (American Lung Association)  
    ... deficiency, the body’s normal production of the AAT protein is impaired, resulting in the destruction of sensitive lung tissue. Learn more about what causes this rare condition.
    https://www.lung.org/.../learn-about-alpha-1-antitrypsin-defiency - External Health Links
  2. Where can I read more about the diseases and traits covered in my direct-to-consumer genetic testing report?: ... 
    ... also called PMM2 -CDG Cystic fibrosis D-bifunctional protein deficiency Dihydrolipoamide ... storage disease type I Hereditary fructose intolerance ...
    https://medlineplus.gov/.../dtcgenetictesting/dtcghrpages - Genetics
  3. Factor X deficiency 
    ... K (some newborns are born with vitamin K deficiency) Buildup of abnormal proteins in the tissues and organs ( amyloidosis ) Severe liver disease Use of medicines that prevent clotting (anticoagulants such ...
    https://medlineplus.gov/ency/article/000553.htm - Medical Encyclopedia
  4. Blood smear 
    ... cells may be due to: Abnormal hemoglobin , the protein in RBCs that carries oxygen (hemoglobinopathies) Deficiency of an enzyme called lecithin cholesterol acyltransferase Iron deficiency Liver disease Spleen removal (splenectomy) Presence of sphere-shaped cells ...
    https://medlineplus.gov/ency/article/003665.htm - Medical Encyclopedia
  5. PSAP gene 
    ... variant metachromatic leukodystrophy) prosaptides SAP1 SAP2 (sphingolipid activator protein-2) SAP_HUMAN SGP-1 (sulfoglycoprotein-1) Tests of PSAP PubMed PROSAPOSIN; PSAP GAUCHER DISEASE, ATYPICAL, DUE TO SAPOSIN C DEFICIENCY; GDSAPC COMBINED SAPOSIN DEFICIENCY; PSAPD KRABBE DISEASE, ATYPICAL, ...
    https://medlineplus.gov/genetics/gene/psap - Genetics
  6. Factor X deficiency 
    ... caused by other disorders such as severe liver disease or systemic amyloidosis, a condition involving the accumulation of abnormal proteins called amyloids. Acquired factor X deficiency can also be caused by certain drugs such ...
    https://medlineplus.gov/genetics/condition/factor-x-deficiency - Genetics
  7. Methemoglobinemia 
    ... amount of methemoglobin is produced. Hemoglobin is the protein in red ... but is not able to release it effectively to body tissues.
    https://medlineplus.gov/ency/article/000562.htm - Medical Encyclopedia
  8. ABCA1 gene 
    ... gene cause a more severe disorder called Tangier disease (described below).Most ABCA1 gene variants that cause familial HDL deficiency change single protein building blocks (amino acids) in the ABCA1 protein. ...
    https://medlineplus.gov/genetics/gene/abca1 - Genetics
  9. Nonalcoholic Fatty Liver Disease (American Academy of Family Physicians)  
    Fatty Liver Disease/Learn More ... Fatty Liver Disease ... American Academy of Family Physicians
    https://familydoctor.org/.../?adfree=true - External Health Links
  10. Metachromatic leukodystrophy 
    ... diffuse, metachromatic form Cerebroside sulphatase deficiency disease Greenfield disease Metachromatic leukoencephalopathy MLD Sulfatide ... National Organization for Rare Disorders (NORD) ...
    https://medlineplus.gov/.../condition/metachromatic-leukodystrophy - Genetics
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