- OMIM ID
-
600273
- OMIM term:
- POLYCYSTIC KIDNEY DISEASE, INFANTILE SEVERE, WITH TUBEROUS SCLEROSIS; PKDTS
- Alternative terms:
-
CHROMOSOME 16p13.3 DELETION SYNDROME, DISTAL
TUBEROUS SCLEROSIS/POLYCYSTIC KIDNEY DISEASE CONTIGUOUS GENE SYNDROME
- (∗) Location:
- 16p13.3
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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