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Diseases
Genes (836)
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MED12
Fg Syndrome
Phyllodes Tumor
ASL
Argininosuccinic Aciduria
POLG
Merrf Syndrome
Balo Concentric Sclerosis
SLC6A19
Hartnup Disease
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
WRN
Werner Syndrome
COL2A1
Collagen, Type Ii, Alpha-1
FLNA
Fg Syndrome
Intestinal Neuronal Dysplasia
Phyllodes Tumor
SLC2A10
Arterial Tortuosity Syndrome
SLC17A5
Salla Disease
SLC2A1
Arterial Tortuosity Syndrome
Werner Syndrome
Glut1 Deficiency
GNAQ
Erdheim–chester Disease
Sturge–weber Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
RHBDF2
Howel–evans Syndrome
GALE
Galactose Epimerase Deficiency
TRNL1
Merrf Syndrome
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
LIPA
Acid Lipase Disease