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Search 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:
Mouse
Zebrafish
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