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 AD 0 0 FBN1 - -
00237 ECTOL1 ectopia lentis, type 1 (ECTOL-1) 129600 AD 22 16 FBN1 - -
00238 GPHYSD2 dysplasia, geleophysic, type 2 (GPHYSD-2) 614185 AD 0 0 FBN1 - -
00240 MASS MASS syndrome (MASS) 604308 AD 1 1 FBN1 - -
05911 MFLS lipodystrophy, Marfan syndrome (MFLS) 616914 AD 1 1 FBN1 - -
00239 MFS Marfan syndrome (MFS) 154700 AD 185 171 FBN1 - autosomal dominant
00127 SSKS stiff skin syndrome (SSKS) 184900 AD 1 0 FBN1 - -
00241 WMS2 Weill-Marchesani syndrome, type 2 (WMS-2) 608328 AD 0 0 FBN1 - -
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