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
00616 PRLTS Perrault syndrome - - 32 32 C10orf12, CLPP, DAP3, ERAL1, HARS2, HSD17B4, LARS2 - -
03558 PRLTS3;DFNB81 Perrault syndrome, type 3 (PRLTS3; DFNB81) 614129 AR 5 5 CLPP - -
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