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6 results
  1. ... KRT5 loss-of-function variants (OMIM 179850 ). KRT14 Naegeli-Franceschetti-Jadassohn syndrome (OMIM 161000 ) & dermatopathia pigmentosa reticularis (OMIM 125595 ) are ...
  2. ... topic><topic ><url >https://medlineplus.gov/genetics/condition/naegeli-franceschetti-jadassohn-syndrome-dermatopathia-pigmentosa-reticularis</url><title >Naegeli-Franceschetti-Jadassohn ...
  3. ... pterygium syndrome: MedlinePlus Genetics (National Library of Medicine) Naegeli-Franceschetti-Jadassohn syndrome/dermatopathia pigmentosa reticularis: MedlinePlus Genetics (National Library of ...
  4. ... other manifestations of IP includes the following disorders: Naegeli syndrome (OMIM 161000 ), a rare autosomal dominant disorder affecting ... hyperkeratosis of the palms and soles. Unlike IP, Naegeli syndrome does not evolve through different stages of skin ...
  5. NLM Digital Collections - Integrated authority file : IAF 
    Publication: [Bethesda, Md.] : U.S. Dept. of Health, Education, and Welfare, Public Health Service, National Institutes of Health, 1974
    ... LEUKEHIA, HYELOCYTIC Naeqeli's leukemia (SYN) X LEUKEBIA, MYELOCYTIC Naegeli's syndrome (SYN) X PIGMENTATION DISORDERS N EYE DISEASES P ...