PMC:1852721 / 69497-69944 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/1852721","sourcedb":"PMC","sourceid":"1852721","source_url":"https://www.ncbi.nlm.nih.gov/pmc/1852721","text":"Table 3 Molecular Defects in Mendelian Disorders (and Somatic Mutations in Neoplasms) (January 29, 2007)\nMapping Type No. Mapped\nLoci in OMIM with at least one known point mutation that causes a disorder or neoplasm 2,002\nMapped disorders for which a causative mutation has been identified 3,345a\nTotal no. of mutations cataloged in OMIM 14,949\na Number of phenotypes labeled with “(3)” in the Disorder field of the Synopsis of the Human Gene Map.","divisions":[{"label":"label","span":{"begin":0,"end":7}},{"label":"caption","span":{"begin":8,"end":104}},{"label":"p","span":{"begin":8,"end":104}},{"label":"table","span":{"begin":105,"end":344}},{"label":"tr","span":{"begin":105,"end":128}},{"label":"th","span":{"begin":105,"end":117}},{"label":"th","span":{"begin":118,"end":128}},{"label":"tr","span":{"begin":129,"end":221}},{"label":"td","span":{"begin":129,"end":215}},{"label":"td","span":{"begin":216,"end":221}},{"label":"tr","span":{"begin":222,"end":296}},{"label":"td","span":{"begin":222,"end":289}},{"label":"td","span":{"begin":290,"end":296}},{"label":"tr","span":{"begin":297,"end":344}},{"label":"td","span":{"begin":297,"end":337}},{"label":"td","span":{"begin":338,"end":344}},{"label":"label","span":{"begin":345,"end":346}}],"tracks":[]}