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Results 71 - 80 of 253 for Blood group B
  1. COL3A1 gene 
    ... the vascular type. Ehlers-Danlos syndrome is a group of disorders that affect the connective tissues that support the skin, bones, blood vessels, and many other organs and tissues. The ...
    https://medlineplus.gov/genetics/gene/col3a1 - Genetics
  2. COL1A2 gene 
    ... the arthrochalasia type. Ehlers-Danlos syndrome is a group of disorders that affect the connective tissues that support the skin, bones, blood vessels, and many other organs and tissues. The ...
    https://medlineplus.gov/genetics/gene/col1a2 - Genetics
  3. COL5A2 gene 
    ... the classical type. Ehlers-Danlos syndrome is a group of disorders that affect the connective tissues that support the skin, bones, blood vessels, and many other organs and tissues. This ...
    https://medlineplus.gov/genetics/gene/col5a2 - Genetics
  4. COL5A1 gene 
    ... the classical type. Ehlers-Danlos syndrome is a group of disorders that affect the connective tissues that support the skin, bones, blood vessels, and many other organs and tissues. This ...
    https://medlineplus.gov/genetics/gene/col5a1 - Genetics
  5. PLOD1 gene 
    ... the kyphoscoliotic type. Ehlers-Danlos syndrome is a group of disorders that affect the connective tissues that support the skin, bones, blood vessels, and many other organs and tissues. The ...
    https://medlineplus.gov/genetics/gene/plod1 - Genetics
  6. TNXB gene 
    ... the hypermobile type. Ehlers-Danlos syndrome is a group of disorders that affect the connective tissues that support the skin, bones, blood vessels, and many other organs and tissues. The ...
    https://medlineplus.gov/genetics/gene/tnxb - Genetics
  7. 3-methylglutaconyl-CoA hydratase deficiency 
    ... they have elevated levels of acid in their blood (metabolic acidosis) and excrete large amounts of acid in their urine (aciduria). 3-methylglutaconyl-CoA hydratase deficiency is one of a group of metabolic disorders that can be diagnosed by ...
    https://medlineplus.gov/...methylglutaconyl-coa-hydratase-deficiency - Genetics
  8. FGFR1 gene 
    ... in the processing of smells by a specialized group of neurons (olfactory neurons). The FGFR1 gene is involved in a type of blood cancer called 8p11 myeloproliferative syndrome. This condition is ...
    https://medlineplus.gov/genetics/gene/fgfr1 - Genetics
  9. NCF1 gene 
    ... Boer M, van Leeuwen K, Koker MY, Wolach B, Roesler J, Malech HL, Holland SM, Gallin JI, Stasia MJ. Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update). Blood Cells Mol Dis. 2010 Apr 15;44(4): ...
    https://medlineplus.gov/genetics/gene/ncf1 - Genetics
  10. NCF4 gene 
    ... Boer M, van Leeuwen K, Koker MY, Wolach B, Roesler J, Malech HL, Holland SM, Gallin JI, Stasia MJ. Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update). Blood Cells Mol Dis. 2010 Apr 15;44(4): ...
    https://medlineplus.gov/genetics/gene/ncf4 - Genetics
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