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Results 31 - 40 of 1,504 for condition
  1. F13A1 gene 
    ... stopping blood loss effectively. More About This Health Condition Several common variations (polymorphisms) in the F13A1 gene have been studied as possible risk factors for diseases involving abnormal blood clotting. The most common F13A1 ...
    https://medlineplus.gov/genetics/gene/f13a1 - Genetics
  2. TPO gene 
    ... TPO gene mutations can cause congenital hypothyroidism, a condition characterized by abnormally low levels of thyroid hormones ... birth. The TPO gene mutations involved in this condition delete, add, or change DNA building blocks (base ...
    https://medlineplus.gov/genetics/gene/tpo - Genetics
  3. COL4A5 gene 
    ... the COL4A5 gene can cause Alport syndrome, a condition characterized by kidney disease, hearing loss, and eye abnormalities. Most of these ... of the eye (retina). More About This Health Condition ASLN ATS CA54 CO4A5_HUMAN collagen IV, alpha- ...
    https://medlineplus.gov/genetics/gene/col4a5 - Genetics
  4. F9 gene 
    ... episodes of abnormal bleeding. More About This Health Condition MedlinePlus Genetics provides information about Warfarin sensitivity More About This Health Condition Several rare mutations in the F9 gene cause ...
    https://medlineplus.gov/genetics/gene/f9 - Genetics
  5. SUMF1 gene 
    ... been found to cause multiple sulfatase deficiency. This condition is apparent at birth or early childhood and ... associated with the less severe cases of the condition, whereas mutations that lead to the production an ...
    https://medlineplus.gov/genetics/gene/sumf1 - Genetics
  6. AIRE gene 
    ... candidiasis-ectodermal dystrophy (APECED). APECED is an inherited condition that affects many of the body's organs. ... in people with APECED. More About This Health Condition MedlinePlus Genetics provides information about Alopecia areata More ...
    https://medlineplus.gov/genetics/gene/aire - Genetics
  7. RDH5 gene 
    ... necessary for normal vision, especially in low-light conditions (night vision). This enzyme is found in a ... have been found to cause fundus albipunctatus, a condition characterized by impaired night vision and whitish-yellow ...
    https://medlineplus.gov/genetics/gene/rdh5 - Genetics
  8. SLC20A2 gene 
    ... found to cause primary familial brain calcification. This condition is characterized by abnormal deposits of calcium (calcification) ... limited to these regions. More About This Health Condition gibbon ape leukemia virus receptor 2 GLVR-2 ...
    https://medlineplus.gov/genetics/gene/slc20a2 - Genetics
  9. UROS gene 
    ... of congenital erythropoietic porphyria. More About This Health Condition Cosynthase HEM4_HUMAN Hydroxymethylbilane hydro-lyase (cyclizing) UROIIIS ...
    https://medlineplus.gov/genetics/gene/uros - Genetics
  10. CASR gene 
    ... Mutations in the CASR gene can cause a condition called autosomal dominant hypocalcemia type 1, which is ... hypoparathyroidism).Most CASR gene mutations involved in this condition change single protein building blocks (amino acids) in ...
    https://medlineplus.gov/genetics/gene/casr - Genetics
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