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
04349 AFPD alpha-fetoprotein deficiency (AFPD) 615969 AR - - AFP - -
04350 HPAFP alpha-fetoprotein, hereditary persistence of (HPAFP) 615970 AD - - AFP - -
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