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This includes the morbid map information sorted by chromosome location. We are determined to keep this website freely accessible. Please contact us if you have specific data requirements that are not met by the files listed above. It is usually most appropriate to cite the actual journal article for the data of interest. Research and educational use of OMIM is encouraged, and single-user academic, non-profit, and governmental agencies can register below for access to the following files without a license. I hereby declare that I will not use or share the data contained in OMIM for any commercial purposes, will not develop a derivative database, nor distribute the data to a third party without first obtaining a license from Johns Hopkins University to do so. User acknowledges and agrees that JHU shall not be liable, directly or indirectly, for any damage or loss direct or indirect relating to User's use of or reliance on such data, software or other content. JHU does not endorse and is not responsible for any data, software or other content available from such sites or resources or their privacy policies.

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  • OMIM Online Mendelian Inheritance in Man
  • OMIM Download Request
  • OMIM Online Mendelian Inheritance in Man

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    - AMYLOID BETA A4 PRECURSOR PROTEIN; APP - AMYLOID OF AGING AND ALZHEIMER DISEASE; AAA;; CEREBRAL VASCULAR AMYLOID. - AMYLOID BETA A4 PRECURSOR PROTEIN; APP - AMYLOID OF. - AMYLOID BETA A4 PRECURSOR PROTEIN-BINDING, FAMILY B, MEMBER 2; APBB2 - FELIKE 1; FE65L1 - APBB2.
    This includes the morbid map information sorted by chromosome location. Expert curators review the literature and organize it to facilitate your work.

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    OMIM Online Mendelian Inheritance in Man

    User shall not copy, reproduce, distribute or create derivative works of or otherwise modify OMIM or any part thereof. Amberger JS, Hamosh A.

    Low levels were also detected in brain, with somewhat higher expression in medulla and spinal cord.

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    App omim
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    - AMYLOID BETA A4 PRECURSOR-LIKE PROTEIN 1; APLP1 - AMYLOID PRECURSOR-LIKE PROTEIN 1;; AMYLOID PRECURSOR-LIKE PROTEIN. - AMYLOID BETA A4 PRECURSOR PROTEIN-BINDING, FAMILY A, MEMBER 3; APBA3 - XLIKE 2; X11L2;; MUNCINTERACTING PROTEIN 3.

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    Mutations in the APP gene can also cause autosomal dominant Alzheimer disease-1 (AD1; ), which shows overlapping clinical and neuropathologic .
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    Unfortunately, it is not free to produce. A Phenotypic Series is a tabular view of genetic heterogeneity of similar phenotypes across the genome. Registering below will initiate this process, and you can expect to hear from the JHU licensing office within 2 business days.

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    OMIM Online Mendelian Inheritance in Man

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