FG SYNDROME 2; FGS2 |
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FG SYNDROME 4; FGS4 |
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FIBRODYSPLASIA OSSIFICANS PROGRESSIVA; FOP |
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FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1; CFEOM1 |
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FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULAR INVOLVEMENT; CFEOM3A |
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FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 5; CFEOM5 |
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FICOLIN 3 DEFICIENCY |
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FILIPPI SYNDROME; FLPIS |
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FISH-EYE DISEASE; FED |
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FLECK RETINA, FAMILIAL BENIGN; FRFB |
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FLOATING-HARBOR SYNDROME; FLHS |
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FOCAL CORTICAL DYSPLASIA, TYPE II; FCORD2 |
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FOCAL DERMAL HYPOPLASIA; FDH |
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FOCAL FACIAL DERMAL DYSPLASIA 3, SETLEIS TYPE; FFDD3 |
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FOCAL SEGMENTAL GLOMERULOSCLEROSIS 1; FSGS1 |
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FOCAL SEGMENTAL GLOMERULOSCLEROSIS 2; FSGS2 |
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FOCAL SEGMENTAL GLOMERULOSCLEROSIS 3, SUSCEPTIBILITY TO; FSGS3 |
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FOCAL SEGMENTAL GLOMERULOSCLEROSIS 4, SUSCEPTIBILITY TO; FSGS4 |
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FOCAL SEGMENTAL GLOMERULOSCLEROSIS 5; FSGS5 |
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FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6; FSGS6 |
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