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
01575 HHT telangiectasia hemorrhagic, hereditary (HHT) - - 72 71 ACVRL1, ENG, GDF2 - -
05522 HHT1 telangiectasia hemorrhagic, hereditary, type 1 (HHT1, Osler-Rendu-Weber disease) 187300 AD 2 - ENG - autosomal dominant
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