3billion
back to listBack to List

F13B

coagulation factor XIII B chain

HCNC Approved Symbol
F13B (HGNC:3534)
Genomic Coordinates
1:197,038,741 - 197,067,260 (1q31.3)
Synonyms
FXIIIB
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Factor XIIIB deficiency
613235AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the F13B gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results