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Results 1 - 10 of 12 for Simple ear
  1. Auriculo-condylar syndrome 
    ... fewer folds and grooves than usual (described as "simple"), narrow ear canals, small skin tags in front of or ...
    https://medlineplus.gov/.../condition/auriculo-condylar-syndrome - Genetics
  2. PACS1 syndrome 
    ... and upper lip (philtrum), widely spaced teeth, and ears that are low-set with fewer folds and grooves than normal (described as "simple"). Abnormalities of other body systems can also occur, ...
    https://medlineplus.gov/genetics/condition/pacs1-syndrome - Genetics
  3. Motion sickness 
    ... otoliths, which are tiny structures in the inner ear that are involved in ... processes the simple sugar glucose and the hormone insulin, which helps ...
    https://medlineplus.gov/genetics/condition/motion-sickness - Genetics
  4. Fibrochondrogenesis 
    ... FS. Molecular pathogenesis of fibrochondrogenesis: is it really simple COL11A1 deficiency? Gene. 2012 Dec 15;511(2): ...
    https://medlineplus.gov/genetics/condition/fibrochondrogenesis - Genetics
  5. Palmoplantar keratoderma with deafness 
    ... a process called oxidative phosphorylation, mitochondria use oxygen, simple sugars, and fatty acids to create adenosine triphosphate ( ... mutation are limited to cells in the inner ear and the skin in this condition. GJB2 MT- ...
    https://medlineplus.gov/.../palmoplantar-keratoderma-with-deafness - Genetics
  6. Mitochondrial DNA 
    ... phosphorylation is a process that uses oxygen and simple sugars to create adenosine triphosphate (ATP), the cell' ... s thirties or forties. It typically affects both ears and worsens gradually over time, making it difficult ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics
  7. COL11A1 gene 
    ... FS. Molecular pathogenesis of fibrochondrogenesis: is it really simple COL11A1 deficiency? Gene. 2012 Dec 15;511(2): ...
    https://medlineplus.gov/genetics/gene/col11a1 - Genetics
  8. Chromosome 22 
    ... similar signs and symptoms as those with a simple deletion.The signs and symptoms of 22q13.3 ... skin tags or pits in front of the ear, unusually formed ears, heart defects, kidney problems, malformations ...
    https://medlineplus.gov/genetics/chromosome/22 - Genetics
  9. ALG12-congenital disorder of glycosylation 
    ... enzyme produced from the ALG12 gene transfers a simple sugar called mannose to growing oligosaccharides at a ...
    https://medlineplus.gov/...lg12-congenital-disorder-of-glycosylation - Genetics
  10. 22q13.3 deletion syndrome 
    ... similar signs and symptoms as those with a simple deletion.Researchers are working to identify all of ...
    https://medlineplus.gov/genetics/condition/22q133-deletion-syndrome - Genetics
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