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Diseases
Genes (674)
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MED12
Fg Syndrome
Phyllodes Tumor
FOXP3
Phyllodes Tumor
Ipex Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
FECH
Erythropoietic Protoporphyria
PQBP1
Renpenning's Syndrome
ABCC9
Cantú Syndrome
UMOD
Medullary Cystic Kidney Disease
UBE3B
Kaufman Oculocerebrofacial Syndrome
GALE
Galactose Epimerase Deficiency
KCNJ8
Cantú Syndrome
DMPK
Myotonic Dystrophy
FLNA
Fg Syndrome
Phyllodes Tumor
TRNL1
Merrf Syndrome
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
CD55
Protein Losing Enteropathy
SLC4A4
Proximal Renal Tubular Acidosis
SYCP3
Spermatogenesis Arrest
PSTPIP1
Pyoderma Gangrenosum
CNBP
Myotonic Dystrophy