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
01270 CDD dysplasia, craniodiaphyseal, autosomal dominant (CDD 122860 AD 0 0 SOST - -
05307 SOST sclerosteosis (SOST) - - 10 10 LRP4, SOST - -
02067 SOST1 sclerosteosis, type 1 (SOST-1) 269500 AR 1 1 SOST - -
01857 VBCH disease, van Buchem (VBCH, hyperostosis corticalis generalisata) 239100 AR 5 4 SOST - -
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