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
04121 AI2A5 amelogenesis imperfecta, hypomaturation type, IIA5 (AI2A5) 615887 AR - - SLC24A4 - -
01682 SHEP6 pigmentation, skin/hair/eye, variation in, type 6 (SHEP-6) 210750 AR 1 1 SLC24A4 - -
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