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Diseases
Genes (1115)
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MED12
Fg Syndrome
Fragile X Syndrome
Phyllodes Tumor
FMR1
Fg Syndrome
Renpenning's Syndrome
Fragile X Syndrome
Rolandic Epilepsy
POLG
Merrf Syndrome
Balo Concentric Sclerosis
FOXP3
Ipex Syndrome
Phyllodes Tumor
TBX5
Holt–oram Syndrome
COL6A1
Bethlem Myopathy
ABCC9
Cantú Syndrome
Hippocampal Sclerosis
FECH
Erythropoietic Protoporphyria
PQBP1
Renpenning's Syndrome
TAF1
Dystonia 3, Torsion, X-Linked
UMOD
Medullary Cystic Kidney Disease
COL6A3
Bethlem Myopathy
COL6A2
Bethlem Myopathy
UBE3B
Kaufman Oculocerebrofacial Syndrome
GALE
Galactose Epimerase Deficiency
KCNJ8
Cantú Syndrome
ACTG2
Berdon Syndrome
DMPK
Myotonic Dystrophy
FLNA
Fg Syndrome
Phyllodes Tumor
TRNL1
Merrf Syndrome