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Results 61 - 70 of 1,314 for the
  1. Craniometaphyseal dysplasia 
    ... condition characterized by thickening (overgrowth) of bones in the skull (cranium) and abnormalities in a region at the end of long bones known as the metaphysis. ...
    https://medlineplus.gov/.../condition/craniometaphyseal-dysplasia - Genetics
  2. Granulomatosis with polyangiitis 
    ... a condition that causes inflammation that primarily affects the respiratory tract (including the lungs and airways) and the kidneys. This disorder is formerly known as Wegener ...
    https://medlineplus.gov/.../granulomatosis-with-polyangiitis - Genetics
  3. Cardiofaciocutaneous syndrome 
    ... is a disorder that affects many parts of the body, particularly the heart (cardio-), facial features (facio-), and the skin and hair (cutaneous). People with this condition ...
    https://medlineplus.gov/.../condition/cardiofaciocutaneous-syndrome - Genetics
  4. Primary myelofibrosis 
    Primary myelofibrosis is a condition characterized by the buildup of scar tissue (fibrosis) in the bone marrow, the tissue that produces blood cells. Because of the fibrosis, the bone marrow is ...
    https://medlineplus.gov/genetics/condition/primary-myelofibrosis - Genetics
  5. Succinyl-CoA:3-ketoacid CoA transferase deficiency 
    ... SCOT) deficiency is an inherited disorder that impairs the body's ability to break down ketones, which are molecules produced in the liver during the breakdown of fats.The signs ...
    https://medlineplus.gov/...-coa3-ketoacid-coa-transferase-deficiency - Genetics
  6. DICER1 syndrome 
    DICER1 syndrome is an inherited disorder that increases the risk of a variety of cancerous and noncancerous ( ... commonly certain types of tumors that occur in the lungs, kidneys, ovaries, and thyroid (a butterfly-shaped ...
    https://medlineplus.gov/genetics/condition/dicer1-syndrome - Genetics
  7. Multiple epiphyseal dysplasia 
    ... disorder of cartilage and bone development primarily affecting the ends of the long bones in the arms and legs (epiphyses). There are two types ... be distinguished by their pattern of inheritance. Both the dominant and recessive types have relatively mild signs ...
    https://medlineplus.gov/.../condition/multiple-epiphyseal-dysplasia - Genetics
  8. Peters anomaly 
    ... eye problems that occur in an area at the front part of the eye known as the anterior segment. The anterior segment consists of structures including the lens, ...
    https://medlineplus.gov/genetics/condition/peters-anomaly - Genetics
  9. Hyperphosphatemic familial tumoral calcinosis 
    ... is a condition characterized by an increase in the levels of phosphate in the blood (hyperphosphatemia) and abnormal deposits of phosphate and calcium (calcinosis) in the body's tissues. Calcinosis typically develops in early ...
    https://medlineplus.gov/...rphosphatemic-familial-tumoral-calcinosis - Genetics
  10. Dandy-Walker malformation 
    ... Walker malformation affects brain development, primarily development of the cerebellum, which is the part of the brain that coordinates movement. In individuals with this ...
    https://medlineplus.gov/genetics/condition/dandy-walker-malformation - Genetics
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