Usher Syndrome, Type IF [PCDH15]: Profound hearing loss and prepubertal onset of retinitis pigmentosa with progressive degeneration of the cells in the retina.
For detailed information about this disease visit : National Institutes of Health (NIH) >
Carrier Frequency by Ethnicity >
What couples should know about how genetics can affect their baby
AboutAbout the JGDCJGDC ProgramsLeadershipMember OrganizationsSupporters
Genetic HeritageEthnicity and Genetic DiseasesEthnicity vs. Expanded Carrier ScreeningCarrier Frequencies by Ethnicity
Carrier ScreeningWhat is Carrier Screening?What screening should be done?Who should be screened?How is screening done?Where is carrier screening done?
Personal StoriesEvanLauren and JonathanEstie Rose, Genetic CounselorRivkyOur DaughtersMorgan
Rabbis and CantorsPrograms for Rabbis and CantorsPrograms for the CommunityPrograms Presented
Medical ProfessionalsPhysicians and Other Medical ProfessionalsJGDC Grand Rounds ProgramResources for Physicians
DiseasesJewish Genetic DiseasesDiseases Common to All Jewish GroupsAshkenazi Jewish DiseasesSephardic-Mizrahi Diseases
Jewish Genetic Disease Consortium1515 Route 202 – #121Pomona, NY 10970855-642-6900info@JewishGeneticDiseases.org