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
03653 CMM8 melanoma, cutaneous, malignant, susceptibility to, type 8 (CMM8) 614456 - 0 0 MITF - -
05224 COMMAD syndrome, COMMAD (coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness) 617306 AR 2 2 MITF - -
01166 TADS syndrome, Tietz albinism-deafness (TADS) 103500 AD 0 0 MITF - -
01605 WS2A syndrome, Waardenburg , type 2A (WS2A) 193510 AD 6 6 MITF - -
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