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Diseases
Genes (814)
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TTPA
Familial Isolated Vitamin E Deficiency
SLC12A6
Andermann Syndrome
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
SLC17A5
Salla Disease
FECH
Erythropoietic Protoporphyria
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
TRNL1
Merrf Syndrome
TRNP
Merrf Syndrome
TRNF
Merrf Syndrome
TP53
Teratoma
Adenoid Cystic Carcinoma
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
PTEN
Teratoma
Thrombophlebitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
MYH11
Berdon Syndrome