All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05559 BCYM brachyolmia (BCYM) - - 19 11 PAPSS2, TRPV4 - -
03196 BCYM4 brachyolmia, type 4, with mild epiphyseal and metaphyseal changes (BCYM-4, spondyloepimetaphyseal dysplasia, Pakistani type) 612847 AR 1 1 PAPSS2 - autosomal recessive
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