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F5
- Factor V Deficiency
- Factor V Leiden Thrombophilia
- Factor V Leiden
- Factor V And Factor Viii, Combined Deficiency Of, With Normal Protein C And Protein C Inhibitor
NGF
- Hereditary Sensory And Autonomic Neuropathy Type V
- Hereditary Sensory And Autonomic Neuropathy Type V
PYGM
- Glycogen Storage Disease Type V
SCN10A
- Atrioventricular Dissociation
- Hereditary Sensory And Autonomic Neuropathy Type V
- Hereditary Sensory And Autonomic Neuropathy Type V
SCN9A
- Hereditary Sensory And Autonomic Neuropathy Type V
- Hereditary Sensory And Autonomic Neuropathy Type V
NTRK1
- Hereditary Sensory And Autonomic Neuropathy Type V
- Hereditary Sensory And Autonomic Neuropathy Type V
SCN11A
- Hereditary Sensory And Autonomic Neuropathy Type V
- Hereditary Sensory And Autonomic Neuropathy Type V
GARS1
- Distal Hereditary Motor Neuropathy Type V
IFITM5
- Osteogenesis Imperfecta, Type V
BSCL2
- Distal Hereditary Motor Neuropathy Type V
POR
- Factor V Leiden
- Cytochrome P450 Oxidoreductase Deficiency
APOA5
- Hyperlipoproteinemia, Type V
GH1
- Isolated Growth Hormone Deficiency, Type V
HOXD13
- Syndactyly, Type V
ATP5F1A
- Mitochondrial Complex V (Atp Synthase) Deficiency, Nuclear Type 4
ATP5F1E
- Mitochondrial Complex V (Atp Synthase) Deficiency, Nuclear Type 3
TMEM70
- Mitochondrial Complex V (Atp Synthase) Deficiency, Nuclear Type 2
ATP6V1B1
- Renal Tubular Acidosis With Deafness
ATPAF2
- Mitochondrial Complex V Deficiency
ATP5F1D
- Mitochondrial Complex V (Atp Synthase) Deficiency, Nuclear Type 5