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Diseases
Genes (820)
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TTPA
Familial Isolated Vitamin E Deficiency
SLC6A19
Hartnup Disease
ATP7B
Wilson's Disease
SLC12A6
Andermann Syndrome
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
SLC17A5
Wilson's Disease
Salla Disease
FAM20A
Enamel-Renal Syndrome
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
TNF
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Tachycardia
Adenoid Cystic Carcinoma
Wilson's Disease
Salla Disease
ACTG2
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
PTEN
Thrombophlebitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
TP53
Adenoid Cystic Carcinoma
Wilson's Disease
MYH11
Berdon Syndrome
DRD2
Tachycardia
Wilson's Disease