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
00616 PRLTS Perrault syndrome - - 32 32 C10orf12, CLPP, DAP3, ERAL1, HARS2, HSD17B4, LARS2 - -
03793 PRLTS2 Perrault syndrome, type 2 (PRLTS2) 614926 AR - - HARS2 - -
05459 USH3 Usher syndrome, type III (USH-3) - - 170 170 CLRN1, HARS - -
00011 USH3B Usher syndrome, type 3B (USH-3B) 614504 AR 5 4 HARS - -
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