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Diseases
Genes (771)
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TTPA
Familial Isolated Vitamin E Deficiency
PYGM
Glycogen Storage Disease V
POLG
Balo Concentric Sclerosis
FAM20A
Polyuria
Enamel-Renal Syndrome
SLC12A6
Andermann Syndrome
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
SLC17A5
Salla Disease
FECH
Erythropoietic Protoporphyria
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
CTNS
Polyuria
Cystinosis
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
PTEN
Thrombophlebitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome