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Diseases
Genes (841)
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ATP7B
Wilson's Disease
TTPA
Familial Isolated Vitamin E Deficiency
FMR1
Renpenning's Syndrome
Fragile X-Associated Tremor/ataxia Syndrome
Fg Syndrome
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
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
Wilson's Disease
Adenoid Cystic Carcinoma
MYH11
Berdon Syndrome
ANXA5
Wilson's Disease
MYLK
Berdon Syndrome
CTNS
Cystinosis
NOTCH1
Adenoid Cystic Carcinoma
Melorheostosis
RB1
Pinealoblastoma
Wilson's Disease
Trilateral Retinoblastoma