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Diseases
Genes (814)
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TTPA
Familial Isolated Vitamin E Deficiency
SLC12A6
Andermann Syndrome
PTEN
Thrombophlebitis
Protein Losing Enteropathy
Silicosis
Adenoid Cystic Carcinoma
MED13L
Congenitally Uncorrected Transposition Of The Great Arteries
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
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
MYH11
Berdon Syndrome
TP53
Silicosis
Adenoid Cystic Carcinoma
MYLK
Berdon Syndrome
ARG1
Silicosis
CTNS
Cystinosis