OMIM Online Mendelian Inheritance in Man

OMIM is a comprehensive, authoritative database that features catalogs of autosomal dominant, autosomal recessive, x-linked, y-linked, and mitochondrial phenotypes. Includes information on human genes and genetic disorders. The full-text, referenced overviews in OMIM contain information on all known mendelian disorders and over 12,000 genes.
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Online Mendelian inheritance in man (OMIM)

OMIM - NCBI

OMIM - Online Mendelian Inheritance in Man