Genomics England
GMS Panels
Panels
Genes and Entities

PLG

plasminogen
OMIM: 173350
PanelMode of inheritanceDetails
4 panels
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Plasminogen deficiency, type I, OMIM:217090, Dysplasminogenemia, OMIM:217090
Green
in Hydrocephalus
R-numbers: R86
Signed-off version 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Plasminogen deficiency, type I, OMIM:217090, Dysplasminogenemia, OMIM:217090
Green
in Primary immunodeficiency or monogenic inflammatory bowel disease
R-numbers: R15
Signed-off version 7.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Angioedema, hereditary, 4, OMIM:619360
Green
in Thrombophilia with a likely monogenic cause
R-numbers: R97
Signed-off version 2.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Plasminogen deficiency, type I, OMIM:217090, Dysplasminogenemia, OMIM:217090