All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01984 - neuropathy, optic, ischemic, nonarteritic anterior, susceptibility to 258660 AR - - GP1BA - -
00143 BSS Bernard-Soulier syndrome 231200 AR 226 16 GP1BA, GP1BB, GP9 - -
01423 BSSA2 Bernard-Soulier syndrome, type A2, autosomal dominant (BSSA-2) 153670 AD 1 1 GP1BA - autosomal dominant
01532 VWDP von Willebrand disease, pseudo (VWDP) 177820 AD 14 13 GP1BA - autosomal dominant
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