All diseases

OMIM ID
228960
OMIM term:
HIGH MOLECULAR WEIGHT KININOGEN DEFICIENCY
Alternative terms:
HMWK DEFICIENCY
KININOGEN DEFICIENCY, HIGH MOLECULAR WEIGHT
FITZGERALD TRAIT KININOGEN DEFICIENCY, TOTAL, INCLUDED
KININOGEN DEFICIENCY, HIGH MOLECULAR WEIGHT AND LOW MOLECULAR WEIGHT, INCLUDED
FLAUJEAC TRAIT, INCLUDED
WILLIAMS TRAIT, INCLUDED
(∗) Location:
3q27.3  
(†) Associated OMIM genes:
KNG1  
(‡) 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/686k33rz