Xanthism (Rufous Albinism)
General: Autosomal recessive; occurs in blacks.
Ocular: Lack of color in iris.
Clinical: Bright copper-red color of skin and hair.
Barnicot NA. Human pigmentation. Man 1957; 57:114-l20.
McKusick VA. Mendelian Inheritance in Man; A Catalog of Human Genes and Genetic Disorders, 12th ed. Baltimore: The Johns Hopkins University Press, 1998.
Online Mendelian Inheritance in Man, OMIM. McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University and National Center for Biotechnology Information, National Library of Medicine, February 12, 2007. World Wide Web URL: https://www.ncbi.nlm.nih.gov/omim/.
Multiple Sulfatase Deficiency [...] |
Asthma (Hayfever) General: Asthma characterized by paroxysms of expiratory dyspnea and wheezing, overinflation of the lungs, cough, and rhonc [...] |
S Sabin-Feldman Syndrome [...] |
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