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Diseases
Genes (668)
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TTPA
Familial Isolated Vitamin E Deficiency
Hyperoxia
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
ASS1
Hyperoxia
Citrullinemia Type I
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
NKX2-6
Persistent Truncus Arteriosus
ACTG2
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
PLXND1
Persistent Truncus Arteriosus
CD55
Protein Losing Enteropathy
PTEN
Persistent Truncus Arteriosus
Thrombophlebitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
MYH11
Berdon Syndrome
TP53
Persistent Truncus Arteriosus
Adenoid Cystic Carcinoma
IGFBP2
Hyperoxia
Adenoid Cystic Carcinoma
CYP1A1
Hyperoxia
MYLK
Berdon Syndrome
CTNS
Cystinosis
NOTCH1
Adenoid Cystic Carcinoma
Melorheostosis