All diseases

8 entries on 1 page. Showing entries 1 - 8.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00236 ACMID dysplasia, acromicric (ACMID) 102370 - 0 0 FBN1 - -
00237 ECTOL-1 ectopia lentis, type 1 (ECTOL-1) 129600 - 22 16 FBN1 - -
00238 GPHYSD-2 dysplasia, geleophysic, type 2 (GPHYSD-2) 614185 - 0 0 FBN1 - -
00240 MASS MASS syndrome (MASS) 604308 - 1 1 FBN1 - -
05911 MFLS syndrome, lipodystrophy, Marfan (MFLS) 616914 AD 1 1 FBN1 - -
00239 MFS syndrome, Marfan (MFS) 154700 - 176 165 FBN1 - autosomal dominant
00127 SSKS stiff skin syndrome (SSKS) 184900 - 1 0 FBN1 - -
00241 WMS-2 Weill-Marchesani syndrome, type 2 (WMS-2) 608328 - 0 0 FBN1 - -
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