All diseases

OMIM ID
266920
OMIM term:
MAINZER-SALDINO SYNDROME; MZSDS
Alternative terms:
CONORENAL SYNDROME
RENAL DYSPLASIA, RETINAL PIGMENTARY DYSTROPHY, CEREBELLAR ATAXIA, AND SKELETAL DYSPLASIA
(∗) Location:
16p13.3  
(†) Associated OMIM genes:
IFT140  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/sm6s4kbt