PLG

plasminogen
OMIM: 173350, Gene2Phenotype

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Red PLG in COVID-19 research Level 2: Viral research Version 1.146	review	Unknown	Sources Literature
Green PLG in Hydrocephalus Level 2: Neurology Version 5.8 Latest signed off version: v5.0 (7 Aug 2024)	review	BIALLELIC, autosomal or pseudoautosomal	Sources NHS GMS Expert Review Green Literature Phenotypes Plasminogen deficiency, type I, OMIM:217090 Dysplasminogenemia, OMIM:217090
Red PLG in Inherited bleeding disorders Level 3: Haemostasis disorders Level 2: Haematological and immunological disorders Version 1.182	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Eligibility statement prior genetic testing BRIDGE Study Tier 1 Gene Phenotypes Plasminogen deficiency, type I, OMIM:217090 Dysplasminogenemia, OMIM:217090
Green PLG in Primary immunodeficiency or monogenic inflammatory bowel disease Level 2: Immunology Version 8.78 Latest signed off version: v8.0 (30 Apr 2025)	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Angioedema, hereditary, 4, OMIM:619360
Amber PLG in Thrombophilia with a likely monogenic cause Level 2: Haematology Version 2.10 Latest signed off version: v2.2 (22 Mar 2023)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber North West GLH Yorkshire and North East GLH London South GLH NHS GMS Wessex and West Midlands GLH Phenotypes Plasminogen deficiency, type I, OMIM:217090 Dysplasminogenemia, OMIM:217090
Green PLG in Fetal anomalies Level 2: Fetal (including NIPD) Version 6.140 Latest signed off version: v6.0 (30 Apr 2025)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes Plasminogen deficiency, type I, OMIM:217090 Dysplasminogenemia, OMIM:217090