All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06564 HLASA ?Hydrops, lactic acidosis, and sideroblastic anemia 617021 AR - - LARS2 - -
03948 ILFS1 liver failure syndrome, infantile, type 1 615438 AR 1 1 LARS - -
00616 PRLTS Perrault syndrome - - 32 32 C10orf12, CLPP, DAP3, ERAL1, HARS2, HSD17B4, LARS2 - -
03893 PRLTS4 Perrault syndrome, type 4 (PRLTS4) 615300 AR 3 3 LARS2 - -
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