All diseases

OMIM ID
263700
OMIM term:
PORPHYRIA, CONGENITAL ERYTHROPOIETIC
Alternative terms:
CEP
GUNTHER DISEASE
UROPORPHYRINOGEN III SYNTHASE DEFICIENCY
UROS DEFICIENCY
(∗) Location:
10q26.1-q26.2  
(†) Associated OMIM genes:
UROS  
(‡) Associated MGI genes:
Uros  

*Loading mouse genes ...

*Loading zebrafish genes ...

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