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Diseases
Genes (753)
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TTPA
Familial Isolated Vitamin E Deficiency
ATP7B
Wilson's Disease
PQBP1
Renpenning's Syndrome
SLC17A5
Wilson's Disease
Salla Disease
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
SLC20A2
Primary Familial Brain Calcification
NGLY1
Ngly1 Deficiency
PDGFRB
Primary Familial Brain Calcification
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
TNF
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Myotonic Dystrophy
Pleural Effusion
Wilson's Disease
Salla Disease
ACTG2
Berdon Syndrome
FLNA
Aneurysm Of Sinus Of Valsalva
Intestinal Neuronal Dysplasia
Fg Syndrome
DMPK
Myotonic Dystrophy
ASS1
Citrullinemia Type I
PDGFB
Primary Familial Brain Calcification
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
ANXA5
Wilson's Disease