All diseases

OMIM ID
250800
OMIM term:
METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE
Alternative terms:
NADH-DEPENDENT METHEMOGLOBIN REDUCTASE DEFICIENCY
NADH-CYTOCHROME b5 REDUCTASE DEFICIENCY
METHEMOGLOBINEMIA, CONGENITAL, AUTOSOMAL RECESSIVE METHEMOGLOBINEMIA, TYPE I, INCLUDED
METHEMOGLOBINEMIA, TYPE II, INCLUDED
NADH-CYTOCHROME b5 REDUCTASE DEFICIENCY, TYPE I, INCLUDED
NADH-CYTOCHROME b5 REDUCTASE DEFICIENCY, TYPE II, INCLUDED
(∗) Location:
22q13.2  
(†) Associated OMIM genes:
CYB5R3  
(‡) 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/29zbd190