All diseases

OMIM ID
224750
OMIM term:
SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS
Alternative terms:
KERATOSIS PALMOPLANTARIS WITH CYSTIC EYELIDS, HYPODONTIA, AND HYPOTRICHOSIS
ECCRINE TUMORS WITH ECTODERMAL DYSPLASIA
(∗) Location:
2q35  
(†) Associated OMIM genes:
WNT10A  
(‡) Associated MGI genes:

*Loading mouse genes ...

*Loading zebrafish genes ...

Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/r8aq5nka