FOXM1

forkhead box M1
OMIM: 602341, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber FOXM1 in Mendeliome


Version 1.2789

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Moyamoya disease, MONDO:0016820

Amber FOXM1 in Stroke


Level 2: Neurology and neurodevelopmental disorders
Version 1.19

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
  • Literature
Phenotypes
  • Moyamoya disease MONDO:0016820

Amber FOXM1 in Cerebral vascular malformations


Level 2: Neurology and neurodevelopmental disorders
Version 1.9

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    • Literature
    Phenotypes
    • Moyamoya disease MONDO:0016820