F5

coagulation factor V
OMIM: 612309, ClinGen, DECIPHER

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green F5 in Bleeding and Platelet Disorders Level 2: Haematological disorders Version 1.52	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Factor V deficiency, MIM# 227400 MONDO:0009210 Thrombophilia due to activated protein C resistance, MIM# 188055 MONDO:0008560 {Thrombophilia, susceptibility to, due to factor V Leiden}, MIM# 188055
Green F5 in Mendeliome Version 1.2302	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Factor V deficiency, MIM# 227400 MONDO:0009210 Thrombophilia due to activated protein C resistance, MIM# 188055 MONDO:0008560 {Thrombophilia, susceptibility to, due to factor V Leiden}, MIM# 188055
Green F5 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.109	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Factor V deficiency, 227400 (3)
Green F5 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 C gene Phenotypes Factor V deficiency MIM# 227400 Thrombophilia due to activated protein C resistance MIM# 188055
Amber F5 in Prepair 1000+ Level 2: Screening Version 1.1566	3 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Mackenzie's Mission Phenotypes Factor V deficiency, 227400 (3)
Red F5 in BabyScreen+ newborn screening Level 2: Screening Version 1.116	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red BabySeq Category C gene Phenotypes Factor V deficiency, MIM# 227400 MONDO:0009210 Thrombophilia due to activated protein C resistance, MIM# 188055 MONDO:0008560 {Thrombophilia, susceptibility to, due to factor V Leiden}, MIM# 188055
Green F5 in Transplant Co-Morbidity Superpanel Level 2: Screening Version 0.18	0 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes MONDO:0009210 Factor V deficiency, MIM# 227400 {Thrombophilia, susceptibility to, due to factor V Leiden}, MIM# 188055 MONDO:0008560 Thrombophilia due to activated protein C resistance, MIM# 188055