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
00362 CSLE lissencephaly, cobblestone (CSLE) - - 5 5 TMEM5 - -
03817 MDDGA10 dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A10 (MDDGA-10) 615041 AR - - TMEM5 - -
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