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
03982 MRT38 mental retardation, autosomal recessive, type 38 (MRT38) 615516 AR 1 1 HERC2 - -
00478 SHEP1 pigmentation, hair, blond/brown - eyes, blue/non-blue, type 1 (SHEP-1, skin/hair/eye pigmentation) 227220 AR - - HERC2, OCA2 - -
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