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
03308 HFE2B hemochromatosis, type 2B (HFE-2B) 613313 AR - - HAMP - -
06213 NEDHILD;MRD40 neurodevelopmental disorder with hypotonia, impaired language, dysmorphic features (MRD40) 616579 AD 1 1 CHAMP1 - -
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