All diseases

OMIM ID
308940
OMIM term:
LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME; DL-ATS
Alternative terms:
LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY
ALPORT SYNDROME AND DIFFUSE LEIOMYOMATOSIS; ATS-DL
CHROMOSOME Xq22.3 CENTROMERIC DELETION SYNDROME
(∗) Location:
Xq22.3  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/atyi9ls4