Facioscapulohumeral muscular dystrophy 1 is a hereditary muscle disorder that primarily affects the muscles of the face, shoulder blades, and upper ar...

Facioscapulohumeral muscular dystrophy 2 is an inherited muscle disorder that primarily affects the muscles of the face, shoulder, and upper arms, lea...

Facioscapulohumeral muscular dystrophy 3, digenic is a neuromuscular condition that primarily affects the muscles of the face, shoulder girdle, and up...

Facioscapulohumeral muscular dystrophy 4, digenic is a neuromuscular condition that primarily affects skeletal muscles of the face, shoulder girdle, a...

Factor 5 excess with spontaneous thrombosis is a hemostatic disorder characterized by an abnormally elevated activity of clotting factor V that predis...

Factor V and factor VIII, combined deficiency of, type 1, is a bleeding disorder caused by mutations in the LMAN1 gene, which leads to deficiencies in...

This condition is a coagulation disorder characterized by a combined deficiency of clotting factors V and VIII while levels of protein C and its inhib...

Factor V deficiency is a coagulation disorder where there is a partial or complete absence of factor V activity in the blood. This condition affects t...

Factor VII and Factor VIII, combined deficiency of is a coagulation disorder that affects the blood clotting process. Although the precise genetic bas...

Factor VII deficiency is a coagulation disorder characterized by reduced or absent activity of factor VII, a protein essential for blood clotting. The...

Factor X deficiency is a coagulation disorder characterized by a partial or complete absence of factor X activity, a protein essential for blood clott...

Factor XI deficiency is a coagulation disorder that results from reduced or absent activity of factor XI, a protein essential for proper blood clottin...

Factor XIII, A subunit, deficiency of is an inherited bleeding disorder that affects the blood’s ability to form stable clots. It is caused by mutatio...

Factor XIII deficiency is a coagulation disorder that may be either acquired or inherited and results from reduced levels and activity of factor XIII,...

FADD-related immunodeficiency is a rare genetic immune disorder that was initially reported in a single consanguineous Pakistani family. People with t...