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1. Deficiencia (medicina): En medicina, una deficiencia es una falta o escasez de una entidad funcional, por un suministro o función inferior a lo normal o necesario. Una persona puede tener deficiencias cromosómicas, deficiencias mentales, deficiencias nutricionales, deficiencias del complemento o deficiencias enzimáticas ... (Medicina) [100%] 2024-05-15
2. DEFICIENS: DEFICIENS is a gene that regulates floral architecture. Examples of DEFICIENS genes include. (Biology) [97%] 2024-01-11 [Plant genes]
3. Chromium deficiency: Articles Most recent articles on Chromium deficiency Most cited articles on Chromium deficiency Review articles on Chromium deficiency Articles on Chromium deficiency in N Eng J Med, Lancet, BMJ Media Powerpoint slides on Chromium deficiency Images of Chromium deficiency Photos ... [88%] 2023-12-30 [Endocrinology] [Gastroenterology]...
4. Biotinidase deficiency: Biotinidase deficiency is an autosomal recessive metabolic disorder in which biotin is not released from proteins in the diet during digestion or from normal protein turnover in the cell. This situation results in biotin deficiency. (Medicine) [88%] 2023-12-31 [Autosomal recessive disorders] [Rare diseases]...
5. NGLY1 deficiency: NGLY1 deficiency is a very rare genetic disorder caused by biallelic pathogenic variants in NGLY1. It is an autosomal recessive disorder. (Medicine) [88%] 2023-11-24 [Genetic diseases and disorders] [Rare diseases]...
6. Iodine deficiency: Iodine deficiency is a lack of the trace element iodine, an essential nutrient in the diet. It may result in metabolic problems such as goiter, sometimes as an endemic goiter as well as congenital iodine deficiency syndrome due to untreated ... (Medicine) [88%] 2024-01-01 [Iodine] [Mineral deficiencies]...
7. Phosphofructokinase deficiency: Phosphofructokinase deficiency is a rare muscular metabolic disorder, with an autosomal recessive inheritance pattern. It may affect humans as well as other mammals (especially dogs). [88%] 2022-09-27 [Inborn errors of carbohydrate metabolism] [Autosomal recessive disorders]...
8. Complement deficiency: Complement deficiency is an immunodeficiency of absent or suboptimal functioning of one of the complement system proteins. Because of redundancies in the immune system, many complement disorders are never diagnosed. [88%] 2023-10-26 [Complement deficiency] [Noninfectious immunodeficiency-related cutaneous conditions]...
9. Folate deficiency (patient information): Overview What are the symptoms? What are the causes?. (Patient information) [88%] 2023-04-08 [Disease] [Gastroenterology]...
10. Molybdenum deficiency (plant disorder): Molybdenum (Mo) deficiency occurs when plant growth is limited because the plant cannot take up sufficient quantities of this essential micronutrient from its growing medium. For crops growing in soil, this may be a result of low concentrations of Mo ... (Chemistry) [88%] 2022-10-23 [Molybdenum]
11. Biotin deficiency: Biotin deficiency is a nutritional disorder which can become serious, even fatal, if allowed to progress untreated. It can occur in people of any age, ancestry, or of either sex. (Medicine) [88%] 2023-12-29 [Vitamin deficiencies]
12. Thiamine deficiency: Thiamine deficiency is a medical condition of low levels of thiamine (vitamin B1). A severe and chronic form is known as beriberi. [88%] 2023-12-29 [Reduplicants] [Vitamin deficiencies]...
13. Copper deficiency: Copper deficiency is defined either as insufficient copper to meet the needs of the body, or as a serum copper level below the normal range. Copper deficiency can have blood related consequences, such as myelodysplasia, anemia, low white blood cell ... (Insufficient level of copper in the body, leading to anaemia and nervous symptoms) [88%] 2023-12-04 [Mineral deficiencies] [Copper in health]...
14. PGM3 deficiency: PGM3 deficiency is a rare genetic disorder of the immune system associated with diminished phosphoglucomutase 3 function. PGM3 is an enzyme which in humans is encoded by gene PGM3. (Medicine) [88%] 2022-11-14 [Genetic diseases and disorders]
15. CD55 deficiency: CD55 deficiency, also called DAF deficiency or CHAPLE syndrome, is a rare genetic disorder of the immune system. CHAPLE stands for "CD55 deficiency with hyper-activation of complement, angiopathic thrombosis, and severe protein-losing enteropathy (PLE)." The disorder usually manifests ... (Medicine) [88%] 2023-08-21 [Rare diseases]
16. Galactokinase deficiency: Galactokinase deficiency is an autosomal recessive metabolic disorder marked by an accumulation of galactose and galactitol secondary to the decreased conversion of galactose to galactose-1-phosphate by galactokinase. The disorder is caused by mutations in the GALK1 gene, located ... [88%] 2023-11-24 [Autosomal recessive disorders] [Inborn errors of carbohydrate metabolism]...
17. DOCK8 deficiency: DOCK8 deficiency, also called DOCK8 immunodeficiency syndrome, is the autosomal recessive form of hyperimmunoglobulin E syndrome, a genetic disorder characterized by elevated immunoglobulin E levels, eosinophilia, and recurrent infections with staphylococcus and viruses. It is caused by a mutation in ... [88%] 2023-10-04 [Genetic diseases and disorders] [Immune system disorders]...
18. Zinc deficiency: Zinc deficiency is a mineral deficiency due to not enough zinc to meet the bodies needs. Symptoms may include diarrhea, hair loss, sexual dysfunction, night blindness, skin rash, increased risk of infections, weight loss, poor healing, abnormal taste, and mental ... [88%] 2023-12-03 [Zinc] [Mineral deficiencies]...
19. Tetrahydrobiopterin deficiency: Tetrahydrobiopterin deficiency (THBD, BH4D) is a rare metabolic disorder that increases the blood levels of phenylalanine. Phenylalanine is an amino acid obtained normally through the diet, but can be harmful if excess levels build up, causing intellectual disability and other ... (Medicine) [88%] 2023-12-22 [Amino acid metabolism disorders] [Autosomal recessive disorders]...
20. Folate deficiency: Home Patient Information Overview Historical Perspective Classification Pathophysiology Causes Differentiating Folate deficiency from other Diseases Epidemiology and Demographics Risk Factors Screening Natural History, Complications and Prognosis Diagnosis Diagnostic Study of Choice History and Symptoms Physical Examination Laboratory Findings Elect. [88%] 2023-03-18 [Disease] [Gastroenterology]...