All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01024 HRFTC hyperferritinemia-cataract syndrome 600886 AD 12 12 FTL - -
04027 LFTD L-ferritin deficiency (LFTD) 615604 AD;AR - - FTL - -
01025 NBIA3 neurodegeneration, with brain iron accumulation, type 3 (NBIA-3) 606159 AD - - FTL - -
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