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
05700 HCIN hyperostosis cranialis interna (HCIN) 144755 AD 1 1 SLC39A14 - -
05698 HMNDYT2 hypermanganesemia with dystonia, type 2 (HMNDYT2) 617013 AR 1 1 SLC39A14 - -
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