All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02125 PCH2A hypoplasia, pontocerebellar, type 2A (PCH-2A) 277470 AR - - TSEN54 - -
01770 PCH4 hypoplasia, pontocerebellar, type 4 (PCH-4) 225753 AR - - TSEN54 - -
05045 PCH5 hypoplasia, pontocerebellar?, type 5 (PCH-5) 610204 AR - - TSEN54 - -
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