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Diseases
Genes (983)
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TTPA
Familial Isolated Vitamin E Deficiency
ATP7B
Wilson's Disease
POLG
Balo Concentric Sclerosis
SLC12A6
Andermann Syndrome
PQBP1
Renpenning's Syndrome
SLC17A5
Wilson's Disease
Salla Disease
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
DMPK
Myotonic Dystrophy
ASS1
Citrullinemia Type I
CD55
Protein Losing Enteropathy
TP53
Adenoid Cystic Carcinoma
Wilson's Disease
Myotonic Dystrophy
PTEN
Thrombophlebitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome