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Diseases
Genes (1054)
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TTPA
Familial Isolated Vitamin E Deficiency
SLC12A6
Andermann Syndrome
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
SLC17A5
Salla Disease
FAM20A
Enamel-Renal Syndrome
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
FGFR4
Acute Respiratory Distress Syndrome
Adenoid Cystic Carcinoma
CCL2
Idiopathic Interstitial Pneumonia
Pulmonary Edema
Acute Respiratory Distress Syndrome
Cystinosis
Melorheostosis
NOS3
Pulmonary Edema
Familial Isolated Vitamin E Deficiency
Acute Respiratory Distress Syndrome
THBD
Idiopathic Interstitial Pneumonia
Acute Respiratory Distress Syndrome
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
PTEN
Idiopathic Interstitial Pneumonia
Thrombophlebitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
MYLK
Acute Respiratory Distress Syndrome
Berdon Syndrome
MYH11
Berdon Syndrome