All conditions under F

All 200+ conditions are caused by changes to specific genes. These genes are shown underneath each condition.

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Conditions

  • Factor V deficiency

    Associated gene: F5

  • Factor VII deficiency

    Associated gene: F7

  • Factor X deficiency

    Associated gene: F10

  • Factor XIII Deficiency
    2 associated genes
    • F13A1
    • F13B
  • Familial Chylomicronaemia Syndrome
    5 associated genes
    • LPL
    • APOC2
    • LMF1
    • APOA5
    • GPIHBP1
  • Familial Haemophagocytic lymphohistiocytosis
    4 associated genes
    • PRF1
    • UNC13D
    • STX11
    • STXBP2
  • Familial hyperphosphataemic tumoral calcinosis
    2 associated genes
    • GALNT3
    • FGF23
  • Familial isolated hypoparathyroidism

    Associated gene: GCM2

  • Familial thrombotic thrombocytopenic purpura

    Associated gene: ADAMTS13

  • Fructose-1,6-bisphosphatase deficiency

    Associated gene: FBP1