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Diseases
Genes (971)
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TTPA
Familial Isolated Vitamin E Deficiency
GJA1
Adenoid Cystic Carcinoma
Oculodentodigital Dysplasia
SLC12A6
Andermann Syndrome
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
SLC17A5
Salla Disease
FECH
Erythropoietic Protoporphyria
PMM2
Pmm2 Deficiency
FAM20A
Enamel-Renal Syndrome
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Hepatitis E
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
DMPK
Myotonic Dystrophy
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
PTEN
Thrombophlebitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
MYH11
Berdon Syndrome
TP53
Adenoid Cystic Carcinoma
Myotonic Dystrophy