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Diseases
Genes (688)
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TTPA
Familial Isolated Vitamin E Deficiency
F12
Factor Xii Deficiency
SLC12A6
Andermann Syndrome
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
SLC17A5
Salla Disease
FAM20A
Enamel-Renal Syndrome
PMM2
Pmm2 Deficiency
FECH
Erythropoietic Protoporphyria
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
PTEN
Thrombophlebitis
Adenoid Cystic Carcinoma
Protein Losing Enteropathy
MYH11
Berdon Syndrome
TP53
Adenoid Cystic Carcinoma
MYLK
Berdon Syndrome