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
00998 - Miller-Dieker lissencephaly syndrome - - 0 0 PAFAH1B1 - -
02112 - Tyrosinemia type I 276700 - 1 1 FAH - -
02654 LIS-1 lissencephaly, type 1 (LIS-1) 607432 - 0 0 PAFAH1B1 - -
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