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Diseases
Genes (743)
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TTPA
Familial Isolated Vitamin E Deficiency
BEST1
Vitelliform Macular Dystrophy
OPA3
Costeff Syndrome
MED12
Fg Syndrome
PQBP1
Renpenning's Syndrome
UMOD
Medullary Cystic Kidney Disease
FAM20A
Enamel-Renal Syndrome
PRPS1
Arts Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
FLNA
Fg Syndrome
Intestinal Neuronal Dysplasia
PTEN
Thrombophlebitis
Adenoid Cystic Carcinoma
Protein Losing Enteropathy
CD55
Protein Losing Enteropathy
ASS1
Citrullinemia Type I
TP53
Adenoid Cystic Carcinoma
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
VEGFA
Corneal Neovascularization
Lymphangiosarcoma
Adenoid Cystic Carcinoma
Subacromial Bursitis
CTNS
Cystinosis