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Results 11 - 20 of 120 for Blood group B
  1. Incontinentia pigmenti 
    ... regulate nuclear factor-kappa-B. Nuclear factor-kappa-B is a group of related proteins that helps protect cells from ...
    https://medlineplus.gov/genetics/condition/incontinentia-pigmenti - Genetics
  2. Anhidrotic ectodermal dysplasia with immune deficiency 
    ... regulate nuclear factor-kappa-B. Nuclear factor-kappa-B is a group of related proteins (a protein complex) that binds ...
    https://medlineplus.gov/...todermal-dysplasia-with-immune-deficiency - Genetics
  3. Ehlers-Danlos syndrome 
    Ehlers-Danlos syndrome is a group of disorders that affect connective tissues supporting the skin, bones, blood vessels, and many other organs and tissues. Defects in connective tissues cause the signs and symptoms of these conditions, which range ...
    https://medlineplus.gov/genetics/condition/ehlers-danlos-syndrome -
  4. Chorea-acanthocytosis 
    ... this condition also have abnormal star-shaped red blood cells (acanthocytosis). This condition is one of a group of conditions called neuroacanthocytoses that involve neurological problems ...
    https://medlineplus.gov/genetics/condition/chorea-acanthocytosis - Genetics
  5. Alport syndrome 
    ... Dotsch J, Muller-Wiefel DE, Hoyer P; Study Group Members of the Gesellschaft fur Padiatrische Nephrologie; Knebelmann B, Pirson Y, Grunfeld JP, Niaudet P, Cochat P, ...
    https://medlineplus.gov/genetics/condition/alport-syndrome - Genetics
  6. 5q minus syndrome 
    ... disorder called myelodysplastic syndrome (MDS). MDS comprises a group of conditions in which immature blood cells fail to develop normally, resulting in too ...
    https://medlineplus.gov/genetics/condition/5q-minus-syndrome - Genetics
  7. Klinefelter syndrome 
    ... risk of developing metabolic syndrome, which is a group of conditions that include high blood glucose levels during prolonged periods without food (fasting), ...
    https://medlineplus.gov/genetics/condition/klinefelter-syndrome - Genetics
  8. Permanent neonatal diabetes mellitus 
    ... chain or the binding of the A and B chains to form insulin, leading to impaired blood glucose control.Permanent neonatal diabetes mellitus can also ... SE, Patch AM, Boustred C, Parrish A, Shields B, Shepherd MH, Hussain K, Kapoor RR, ... Group; Hattersley AT, Ellard S. Insulin mutation screening in ...
    https://medlineplus.gov/.../permanent-neonatal-diabetes-mellitus - Genetics
  9. Oral-facial-digital syndrome 
    ... M, Novelli V, Giorgio G, Barra A, Franco B; Oral-Facial-Digital Type I (OFDI) Collaborative Group. Mutational spectrum of the oral-facial-digital type ...
    https://medlineplus.gov/.../condition/oral-facial-digital-syndrome - Genetics
  10. Congenital nephrotic syndrome 
    ... JA, MacDonald J, Saisawat P, Ashraf S, Ovunc B, Zenker M, Hildebrandt F; Gesselschaft fur Paediatrische Nephrologie (GPN) Study Group. Nineteen novel NPHS1 mutations in a worldwide cohort ...
    https://medlineplus.gov/.../condition/congenital-nephrotic-syndrome - Genetics
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