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Diseases
Genes (815)
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TTPA
Familial Isolated Vitamin E Deficiency
SLC12A6
Andermann Syndrome
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
SLC17A5
Salla Disease
ASS1
Uveitis
Citrullinemia Type I
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
SERPINF1
Uveitis
Adenoid Cystic Carcinoma
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
CD55
Protein Losing Enteropathy
PTEN
Thrombophlebitis
Uveitis
Protein Losing Enteropathy
Adenoid Cystic Carcinoma
MYH11
Berdon Syndrome
AQP1
Uveitis
Adenoid Cystic Carcinoma
MYLK
Berdon Syndrome
TP53
Adenoid Cystic Carcinoma
CTNS
Cystinosis