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Diseases
Genes (840)
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ATP7B
Wilson's Disease
TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
TNF
Callosity
Myotonic Dystrophy
Wilson's Disease
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Pleural Effusion
ACTG2
Berdon Syndrome
FLNA
Aneurysm Of Sinus Of Valsalva
Intestinal Neuronal Dysplasia
Fg Syndrome
DMPK
Myotonic Dystrophy
ASS1
Citrullinemia Type I
PDGFB
Callosity
Primary Familial Brain Calcification
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
ANXA5
Wilson's Disease
IL6
Callosity
Myotonic Dystrophy
Wilson's Disease
Familial Isolated Vitamin E Deficiency
Pleural Effusion
CTNS
Cystinosis