All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00115 CRMCC microangiopathy, cerebroretinal, with calcifications and cysts (CRMCC, Coats plus syndrome) 612199 AR 33 32 CTC1, OBFC1, TEN1 - -
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