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
00059 EXT2 Exostoses, multiple, type 2 133701 - 0 0 EXT2 - -
00058 SSMS Seizures, scoliosis, and macrocephaly syndrome 616682 - 0 0 EXT2 - -
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