FGG

fibrinogen gamma chain
OMIM: 134850, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green FGG in Bleeding and Platelet Disorders Level 2: Haematological disorders Version 1.43	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Afibrinogenaemia, congenital, MIM# 202400 Hypofibrinogenaemia, congenital, MIM# 202400 Dysfibrinogenemia, congenital, MIM# 616004
Green FGG in Mendeliome Version 1.1891	review	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes congenital fibrinogen deficiency MONDO:0018060
Green FGG in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.109	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Afibrinogenemia, congenital, 202400 (3)
Green FGG in Additional findings_Paediatric Level 2: Screening Version 0.278	review	BIALLELIC, autosomal or pseudoautosomal	Sources BabySeq Category A gene Expert Review Green Phenotypes Afibrinogenaemia
Green FGG in Prepair 1000+ Level 2: Screening Version 1.9	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Afibrinogenemia, congenital, 202400 (3)
Green FGG in BabyScreen+ newborn screening Level 2: Screening Version 1.113	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green BabySeq Category A gene Phenotypes Afibrinogenemia, congenital, MIM# 202400 Tags treatable haematological
Green FGG in Transplant Co-Morbidity Superpanel Level 2: Screening Version 0.18	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Afibrinogenaemia, congenital, MIM# 202400 Hypofibrinogenaemia, congenital, MIM# 202400 Dysfibrinogenemia, congenital, MIM# 616004