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
01262 DA9;CCA arthrogryposis, distal, type 9 (DA-9, contractural arachnodactyly, congenital (CCA)) 121050 AD 4 3 FBN2 - -
04468 EOMD macular degeneration, early-onset (EOMD) 616118 AD 0 0 FBN2 - -
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