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
00475 - albinism, ocular, with sensorineural deafness (Waardenburg syndrome, (WS-2OA)) 103470 - - - MITF, TYR - -
03653 CMM-8 melanoma, cutaneous, malignant, susceptibility to, type 8 (CMM-8) 614456 - - - MITF - -
01166 Tietz Tietz syndrome 103500 - - - MITF - -
01605 WS-2A Waardenburg syndrome, type 2A (WS-2A) 193510 - - - MITF - -
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