LMAN1

lectin, mannose binding 1
OMIM: 601567, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green LMAN1 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
  • Combined factor V and VIII deficiency, MIM# 227300
  • MONDO:0009206

Green LMAN1 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Combined factor V and VIII deficiency, MIM# 227300
  • MONDO:0009206

Green LMAN1 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
  • Combined factor V and VIII deficiency, 227300 (3)

Green LMAN1 in Prepair 1000+


Level 2: Screening
Version 1.9

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • Combined factor V and VIII deficiency, 227300 (3)

Green LMAN1 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
  • MONDO:0009206
  • Combined factor V and VIII deficiency, MIM# 227300