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
04287 - myopathy, myofibrillar, fatal infantile hypertrophy, alpha-B crystallin-related 613869 AR 0 0 CRYAB - -
03848 CMD1II cardiomyopathy, dilated, type 1II (CMD-1II) 615184 AD 0 0 CRYAB - -
03424 CTRCT16;CTPP2 cataract, type 16 (CTRCT-16, cataract, posterior polar, type 2 (CTPP-2)) 613763 AD;AR 6 6 CRYAB - -
02797 MFM2 myopathy, myofibrillar, type 2 (MFM-2) 608810 AD 0 0 CRYAB - -
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