Microspherophakia with Hernia
General: Autosomal dominant.
Ocular: Microspherophakia; glaucoma 646g61g .
Clinical: Inguinal hernia.
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/.
Neurilemoma (Schwannoma; Neurinoma) General: Slow [...] |
Infantile Type of Neuronal Ceroid Lipofuscinosis (Ceroid Lipofuscinosis; Hagberg-Santavuori Syndrome; Haltia-Santavuori Syndrome; Santavuori-Haltia [...] |
Histoplasmosis (Histoplasmosis Choroiditis; Histoplasmosis Maculopathy; Presumed Ocular Histoplasmosis Syndrome) [...] |
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