All diseases

OMIM ID
214100
OMIM term:
ZELLWEGER SYNDROME; ZS
Alternative terms:
CEREBROHEPATORENAL SYNDROME
CHR SYNDROME
ZWS
(∗) Location:
12p13.31   1p36.22   1p36.32   1q23.2   22q11.21   2p16.1   6q24.2   7q21.2  
(†) Associated OMIM genes:
PEX1   PEX10   PEX13   PEX14   PEX19   PEX26   PEX3   PEX5  
(‡) Associated MGI genes:
Pex11a   Pex11b   Pex13   Pex2   Pex5  

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* quick link - http://q.sanger.ac.uk/h4el2z0g