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
01525 THPH3 thrombophilia, hereditary, due to protein C deficiency, autosomal dominant (THPH3) 176860 AD 1 1 PROC - -
03118 THPH4 thrombophilia, hereditary, due to protein C deficiency, autosomal recessive (THPH4) 612304 AR - - PROC - -
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