Home Page

Orphanet

References

OMIM

Gene

GeneReviews

HGMD

HGNC

GENATLAS PHENOTYPE

last update : 01-03-2017

Symbol	PLG
Location	6q26
Name	conjunctivitis, ligneous
Corresponding gene	PLG
Main clinical features	initial pseudomembranes on the palpebral surfaces is usually the initial and most common manifestation of type I congenital plasminogen deficiency lesions may be triggered by local injury and/or infection and often recur after local excision
Genetic determination	autosomal recessive
Function/system disorder	eye
Type	disease

Gene product

Name	plasminogen (PLG)

Remark(s)