All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05886 PEBEL encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy (PEBEL) - - 1 - APOA1BP, CARKD - -
05885 PEBEL2 encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, type 2 (PEBEL2) 618321 AR - - CARKD - -
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