All diseases

OMIM ID
102500
OMIM term:
HAJDU-CHENEY SYNDROME; HJCYS
Alternative terms:
ACROOSTEOLYSIS WITH OSTEOPOROSIS AND CHANGES IN SKULL AND MANDIBLE
CHENEY SYNDROME
ARTHRODENTOOSTEODYSPLASIA
SERPENTINE FIBULA-POLYCYSTIC KIDNEY SYNDROME; SFPKS
(∗) Location:
1p12-p11  
(†) Associated OMIM genes:
NOTCH2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/k29n90x4