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
00084 ACMICD ACROMICRIC DYSPLASIA 102370 AD - - FBN1 - -
00085 ECTOL1 ECTOPIA LENTIS 1, ISOLATED, AUTOSOMAL DOMINANT 129600 AD - - FBN1 - -
00086 GPHYSD2 GELEOPHYSIC DYSPLASIA 2 614185 AD - - FBN1 - -
00088 MASSS MASS SYNDROME 604308 AD - - FBN1 - -
00087 MFLS MARFANOID-PROGEROID-LIPODYSTROPHY SYNDROME 616914 AD - - FBN1 - -
00058 MFS1 MARFAN SYNDROME, TYPE I 154700 - - - FBN1 - -
00089 SSKS STIFF SKIN SYNDROME 184900 - - - FBN1 - -
00090 WMS2 WEILL-MARCHESANI SYNDROME 2 608328 AD - - FBN1 - -
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