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
00973 - Melorheostosis with osteopoikilosis 155950 - 0 0 LEMD3 - -
00972 BOS Buschke-Ollendorff syndrome (BOS) 166700 - 0 0 LEMD3 - -
05560 CTRCT-46 cataract, type 46, juvenile-onset (CTRCT-46) 212500 - 0 0 LEMD2 - autosomal recessive
02249 EDMD-1 dystrophy, muscular, Emery-Dreifuss, type 1, X-linked (EDMD-1) 310300 - 0 0 EMD - -
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