PanelApp
  1. Genes and Genomic Entities
  2. PLG

PLG

plasminogen
OMIM: 173350, Gene2Phenotype

9 panels

Panel Reviews Mode of inheritance Details
9 panels

Amber PLG in Bleeding and Platelet Disorders


Level 2: Haematological disorders
Version 1.62

2 reviews BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Expert Review
Phenotypes
  • Plasminogen deficiency, type I
  • Dysplasminogenemia
  • MIM#217090

Green PLG in Hydrocephalus_Ventriculomegaly


Level 2: Neurology and neurodevelopmental disorders
Version 0.132

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Plasminogen deficiency, type I, MIM# 217090

Green PLG in Mendeliome


Version 1.3512

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Hereditary angioedema-4 (HAE4), MIM#619360
  • Plasminogen deficiency, type I, MIM# 217090

Green PLG in Hereditary angioedema


Level 2: Immunological disorders
Version 1.11

Component of the following Super Panels:

  • Immunological disorders_SuperPanel

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Hereditary angioedema-4 (HAE4), MIM#619360

    Green PLG in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.110

    		0 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Plasminogen deficiency, type I, 217090 (3)

    Green PLG in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    		1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • BabySeq Category A gene
    Phenotypes
    • Hereditary angioedema-4 (HAE4), MIM#619360
    • Plasminogen deficiency, type I, MIM# 217090

    Green PLG in Fetal anomalies


    Version 1.465

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    • Victorian Clinical Genetics Services
    Phenotypes
    • Plasminogen deficiency, type I, MIM# 217090
    • Hydrocephalus

    Green PLG in Prepair 1000+


    Level 2: Screening
    Version 2.14

    		2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Plasminogen deficiency, type I, 217090 (3)

    Green PLG in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.140

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • BabySeq Category A gene
    Phenotypes
    • Plasminogen deficiency, type I, MIM# 217090
    Tags
    • treatable
    • haematological