| ℹ️ Description: | OMIM is a comprehensive, authoritative, and timely compendium of human genes and genetic phenotypes. The full-text, referenced overviews in OMIM contain information on all known mendelian disorders and over 12,000 genes. OMIM focuses on the relationship between phenotype and genotype. |
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| 🗃️ Resource type: | dataset |
| 🏷️ Keywords: | gene, gene expression |
| 🏛️ Organization: | NCBI; McKusick-Nathans Institute of Genetic Medicine; Johns Hopkins University |
| 🏠️ Website: | http://www.ncbi.nlm.nih.gov/omim/ |
| 🥇 Preferred prefix: | omim |
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| 🥈 Alternative prefixes: | mim |
| 🖇️ Alternative base URI: | http://europe.omim.org/entry/#http://us-east.omim.org/entry/#http://omim.org/entry/# |
| 🔣 Identifier Regex: | ^[*#+%^]?\d{6}$ |
| 📋️ Example Identifier: | 603903 |
| 🗜️ Template URL: | http://www.ncbi.nlm.nih.gov/omim/$id |