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Diseases
Genes (667)
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TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
ACVR2B
Situs Ambiguus
Takayasu's Arteritis
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
MMP21
Situs Ambiguus
ZIC3
Situs Ambiguus
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
PTEN
Thrombophlebitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
MYH11
Berdon Syndrome
NODAL
Situs Ambiguus
CFAP53
Situs Ambiguus
LEFTY2
Situs Ambiguus
MYLK
Berdon Syndrome
TP53
Adenoid Cystic Carcinoma