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Diseases
Genes (919)
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TTPA
Familial Isolated Vitamin E Deficiency
ATP7B
Wilson's Disease
PQBP1
Renpenning's Syndrome
Pectus Excavatum
MED12
Fg Syndrome
Pectus Excavatum
SLC12A6
Andermann Syndrome
SLC17A5
Wilson's Disease
Salla Disease
FAM20A
Enamel-Renal Syndrome
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
Pectus Excavatum
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
TRNL1
Merrf Syndrome
DMPK
Myotonic Dystrophy
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
ASS1
Citrullinemia Type I
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
ANXA5
Phototoxicity
Wilson's Disease