HLD15 is a new type for the ULF’s list of leukodystrophies. We are working on creating a type description and will update this page when it has been completed. Our type descriptions are written and edited by leukodystrophy professionals from all over the world – including our Medical and Scientific Advisory Board, Leukodystrophy Patient Advocacy Groups, and pharmaceutical partners.

Click here to view the OMIM summary of HLD15.

OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions. OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University. Copyright® 1966-2022 Johns Hopkins University.”