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
03677 IBGC calcification, basal ganglia, idiopathic (IBGC) 614540 - 11 11 SLC20A2 - -
01699 IBGC1 calcification, basal ganglia, idiopathic, type 1 (IBGC-1, Fahr's syndrome) 213600 AD 25 25 SLC20A2 - autosomal dominant
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