All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01271 CDHS craniofacial deafness hand syndrome (CDHS) 122880 AD 2 2 PAX3 - -
02059 RMS2 rhabdomyosarcoma, type 2 (RMS2) 268220 SMo - - FOXO1, PAX3, PAX7 - -
05667 WS Waardenburg syndrome (WS) - - 342 340 EDNRB, PAX3, SOX10 - -
01604 WS1 Waardenburg syndrome, type 1 (WS1) 193500 AD 14 10 PAX3 - -
01408 WS3 Waardenburg syndrome, type 3 (WS3) 148820 AD;AR - - PAX3 - -
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