Link to this page
MedlinePlus Health Topics
| Id | http://purl.bioontology.org/ontology/MEDLINEPLUS/C2939465
http://purl.bioontology.org/ontology/MEDLINEPLUS/C2939465
|
|---|---|
| Preferred Name | G6PDD |
| Definitions |
<p>Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a genetic disorder that is most common in males. About 1 in 10 African American males in the United States has it. G6PD deficiency mainly affects <a href="https://medlineplus.gov/blood.html">red blood cells</a>, which carry oxygen from the lungs to tissues throughout the body. The most common medical problem it can cause is <a href="https://medlineplus.gov/anemia.html">hemolytic anemia</a>. That happens when red blood cells are destroyed faster than the body can replace them.</p> <p>If you have G6PD deficiency, you may not have symptoms. Symptoms happen if your red blood cells are exposed to certain chemicals in food or medicine, certain bacterial or viral infections, or stress. They may include:</p><ul> <li>Paleness</li> <li><a href="https://medlineplus.gov/jaundice.html">Jaundice</a></li> <li>Dark urine</li> <li>Fatigue</li> <li><a href="https://medlineplus.gov/breathingproblems.html">Shortness of breath</a></li> <li>Enlarged spleen</li> <li>Rapid heart rate</li> </ul> <p>A blood test can tell if you have it. Treatments include medicines to treat infection, avoiding substances that cause the problem with red blood cells, and sometimes transfusions.</p> <p class="">NIH: National Library of Medicine</p>
Glucose-6-phosphate dehydrogenase deficiency is a genetic disorder that affects red blood cells, which carry oxygen from the lungs to tissues throughout the body. In affected individuals, a defect in an enzyme called glucose-6-phosphate dehydrogenase causes red blood cells to break down prematurely. This destruction of red blood cells is called hemolysis.~The most common medical problem associated with glucose-6-phosphate dehydrogenase deficiency is hemolytic anemia, which occurs when red blood cells are destroyed faster than the body can replace them. This type of anemia leads to paleness, yellowing of the skin and whites of the eyes (jaundice), dark urine, fatigue, shortness of breath, and a rapid heart rate. In people with glucose-6-phosphate dehydrogenase deficiency, hemolytic anemia is most often triggered by bacterial or viral infections or by certain drugs (such as some antibiotics and medications used to treat malaria). Hemolytic anemia can also occur after eating fava beans or inhaling pollen from fava plants (a reaction called favism).~Glucose-6-phosphate dehydrogenase deficiency is also a significant cause of mild to severe jaundice in newborns. Many people with this disorder, however, never experience any signs or symptoms and are unaware that they have the condition.
|
| Synonyms |
Glucose-6-phosphate dehydrogenase deficiency
Deficiency of glucose-6-phosphate dehydrogenase
Glucose 6 phosphate dehydrogenase deficiency
G6PD deficiency
G6PD Deficiency
Glucose-6-phosphate Dehydrogenase Deficiency
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | <p>Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a genetic disorder that is most common in males. About 1 in 10 African American males in the United States has it. G6PD deficiency mainly affects <a href="https://medlineplus.gov/blood.html">red blood cells</a>, which carry oxygen from the lungs to tissues throughout the body. The most common medical problem it can cause is <a href="https://medlineplus.gov/anemia.html">hemolytic anemia</a>. That happens when red blood cells are destroyed faster than the body can replace them.</p> <p>If you have G6PD deficiency, you may not have symptoms. Symptoms happen if your red blood cells are exposed to certain chemicals in food or medicine, certain bacterial or viral infections, or stress. They may include:</p><ul> <li>Paleness</li> <li><a href="https://medlineplus.gov/jaundice.html">Jaundice</a></li> <li>Dark urine</li> <li>Fatigue</li> <li><a href="https://medlineplus.gov/breathingproblems.html">Shortness of breath</a></li> <li>Enlarged spleen</li> <li>Rapid heart rate</li> </ul> <p>A blood test can tell if you have it. Treatments include medicines to treat infection, avoiding substances that cause the problem with red blood cells, and sometimes transfusions.</p> <p class="">NIH: National Library of Medicine</p> Glucose-6-phosphate dehydrogenase deficiency is a genetic disorder that affects red blood cells, which carry oxygen from the lungs to tissues throughout the body. In affected individuals, a defect in an enzyme called glucose-6-phosphate dehydrogenase causes red blood cells to break down prematurely. This destruction of red blood cells is called hemolysis.~The most common medical problem associated with glucose-6-phosphate dehydrogenase deficiency is hemolytic anemia, which occurs when red blood cells are destroyed faster than the body can replace them. This type of anemia leads to paleness, yellowing of the skin and whites of the eyes (jaundice), dark urine, fatigue, shortness of breath, and a rapid heart rate. In people with glucose-6-phosphate dehydrogenase deficiency, hemolytic anemia is most often triggered by bacterial or viral infections or by certain drugs (such as some antibiotics and medications used to treat malaria). Hemolytic anemia can also occur after eating fava beans or inhaling pollen from fava plants (a reaction called favism).~Glucose-6-phosphate dehydrogenase deficiency is also a significant cause of mild to severe jaundice in newborns. Many people with this disorder, however, never experience any signs or symptoms and are unaware that they have the condition. |
|---|---|
| altLabel |
Glucose-6-phosphate dehydrogenase deficiency
Deficiency of glucose-6-phosphate dehydrogenase
Glucose 6 phosphate dehydrogenase deficiency
G6PD deficiency
G6PD Deficiency
Glucose-6-phosphate Dehydrogenase Deficiency
See more
See less
|
| prefLabel | G6PDD
|
| Associated condition of | |
| DB XR ID | GTR:C2720289~ICD-10-CM:D55.0~MeSH:D005955~OMIM:305900~SNOMED CT:124134002~SNOMED CT:62403005
|
| Mapped from | |
| Inheritance | x:X-linked
|
| Inverse of RQ | |
| Mapped to | |
| type | |
| tui | T047
|
| Related to | |
| Date created | 08/06/2013
|
| notation | C2939465
|
| Scope Statement | Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a genetic disorder that is most common in males. Learn about symptoms, diagnosis and treatment.https://medlineplus.gov/g6pddeficiency.html
|
| Semantic type UMLS property | |
| Inverse of SY | |
| cui | C2939465
|
| MP OTHER LANGUAGE URL | Spanish https://medlineplus.gov/spanish/g6pddeficiency.html
|
| subClassOf |
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |