All diseases

OMIM ID
181500
OMIM term:
SCHIZOPHRENIA; SCZD
Alternative terms:

(∗) Location:
10q22.3   11p14.1   11q14-q21   12q24.11   13q14.2   13q32   13q33.2   14q32.33   18p   1p36.2   1p36.22   1q32.1   1q42.2   22q11.21   22q12.3   3p25.2   3q13.31   5q23-q35   6p22.3   6p23   6q13-q26   8p21  
(†) Associated OMIM genes:
CHI3L1   COMT CATECHOL-O-METHYLTRANSFERASE ACTIVITY, LOW, IN RED CELLS, INCLUDED   DISC1   DRD3   GPR48   HTR2A   MTHFR   RTN4R   SYN2  
(‡) Associated MGI genes:
Akt1   Avpr1a   Chst3   Cplx2   Ctsc   Disc1   Grin1   Lrrtm1   Mdk   Mtap6   Nr4a2   Nrg1   Nrxn1   Plcb1   Ppm1g   Slc6a3   Snap25   Srr   Taar1   Zic2   ckr  

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* quick link - http://q.sanger.ac.uk/t5wllfth