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Results 1 - 10 of 11 for Orange
  1. Tangier disease 
    ... hypertriglyceridemia); disturbances in nerve function (neuropathy); and enlarged, orange-colored tonsils. Affected individuals often develop atherosclerosis, which ...
    https://medlineplus.gov/genetics/condition/tangier-disease - Genetics
  2. Pseudoxanthoma elasticum 
    ... back of the eye) known as peau d'orange. Another eye abnormality known as angioid streaks occurs ...
    https://medlineplus.gov/genetics/condition/pseudoxanthoma-elasticum - Genetics
  3. Familial HDL deficiency 
    ... symptoms, such as disturbances in nerve function; enlarged, orange-colored tonsils; and clouding of the clear covering ...
    https://medlineplus.gov/genetics/condition/familial-hdl-deficiency - Genetics
  4. Epidermal nevus 
    ... sebaceous. Nevi in this group are waxy, yellow-orange patches of skin, usually on the scalp or ...
    https://medlineplus.gov/genetics/condition/epidermal-nevus - Genetics
  5. Rotor syndrome 
    ... blood cells are broken down. It has an orange-yellow tint, and buildup of this substance can ...
    https://medlineplus.gov/genetics/condition/rotor-syndrome - Genetics
  6. DOCK8 immunodeficiency syndrome 
    ... Hanson IC, Albert MH, Geha RS, Renner ED, Orange JS. Defective actin accumulation impairs human natural killer ...
    https://medlineplus.gov/.../dock8-immunodeficiency-syndrome - Genetics
  7. Gilbert syndrome 
    ... in the blood (hyperbilirubinemia). Bilirubin, which has an orange-yellow tint, is produced when red blood cells ...
    https://medlineplus.gov/genetics/condition/gilbert-syndrome - Genetics
  8. Crigler-Najjar syndrome 
    ... in their blood (unconjugated hyperbilirubinemia).Bilirubin has an orange-yellow tint, and hyperbilirubinemia causes yellowing of the ...
    https://medlineplus.gov/genetics/condition/crigler-najjar-syndrome - Genetics
  9. Dubin-Johnson syndrome 
    ... of old red blood cells and has an orange-yellow tint.ABCC2 gene mutations result in the ...
    https://medlineplus.gov/genetics/condition/dubin-johnson-syndrome - Genetics
  10. PGM3-congenital disorder of glycosylation 
    ... Mendelian Genomics; Boerwinkle EA, Gibbs RA, Lupski JR, Orange JS, Lausch E, Hanson IC. PGM3 mutations cause ...
    https://medlineplus.gov/...pgm3-congenital-disorder-of-glycosylation - Genetics
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