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Diseases
Genes (1182)
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GALT
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency
GALE
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency
ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
FOXP3
Ipex Syndrome
TNFAIP3
Haploinsufficiency Of A20
SLC2A10
Arterial Tortuosity Syndrome
Aneurysm
FLNA
Multiple Epiphyseal Dysplasia
Intestinal Neuronal Dysplasia
Fg Syndrome
MED12
Squamous-Cell Carcinoma Of The Lung
Fg Syndrome
PQBP1
Renpenning's Syndrome
PRPS1
Arts Syndrome
GALK1
Galactose-1-Phosphate Uridylyltransferase Deficiency
Galactose Epimerase Deficiency
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
COL9A1
Multiple Epiphyseal Dysplasia
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
FGFR2
Squamous-Cell Carcinoma Of The Lung
SOST
Multiple Epiphyseal Dysplasia
Craniodiaphyseal Dysplasia